Sensitivity and Specificity Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 18.98 | 509 | 30 |
Amyloidosis, Hereditary [description not available] | 0 | 2.83 | 3 | 0 |
Dermatoses [description not available] | 0 | 17.3 | 379 | 6 |
Genetic Skin Diseases [description not available] | 0 | 7.93 | 30 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 17.3 | 379 | 6 |
Amyloidosis, Familial Diseases in which there is a familial pattern of AMYLOIDOSIS. | 0 | 2.83 | 3 | 0 |
Esophageal Squamous Cell Carcinoma A carcinoma that originates usually from cells on the surface of the middle and lower third of the ESOPHAGUS. Tumor cells exhibit typical squamous morphology and form large polypoid lesions. Mutations in RNF6, LZTS1, TGFBR2, DEC1, and WWOX1 genes are associated with this cancer. | 0 | 3.67 | 8 | 0 |
Cancer of Esophagus [description not available] | 0 | 12.17 | 180 | 4 |
Foreign-Body Granuloma [description not available] | 0 | 2.71 | 3 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 12.17 | 180 | 4 |
Colorectal Cancer [description not available] | 0 | 13.36 | 185 | 6 |
Bowel Diseases, Inflammatory [description not available] | 0 | 5.58 | 9 | 0 |
Colorectal Neoplasms Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI. | 0 | 13.36 | 185 | 6 |
Inflammatory Bowel Diseases Chronic, non-specific inflammation of the GASTROINTESTINAL TRACT. Etiology may be genetic or environmental. This term includes CROHN DISEASE and ULCERATIVE COLITIS. | 0 | 5.58 | 9 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 3.09 | 5 | 0 |
Kahler Disease [description not available] | 0 | 3.94 | 13 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 3.09 | 5 | 0 |
Multiple Myeloma A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY. | 0 | 3.94 | 13 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 18.8 | 954 | 10 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 18.8 | 954 | 10 |
Lichen Planus, Oral Oral lesions accompanying cutaneous lichen planus or often occurring alone. The buccal mucosa, lips, gingivae, floor of the mouth, and palate are usually affected (in a descending order of frequency). Typically, oral lesions consist of radiating white or gray, velvety, threadlike lines, arranged in a reticular pattern, at the intersection of which there may be minute, white, elevated dots or streaks (Wickham's striae). (Jablonski, Illustrated Dictionary of Dentistry) | 0 | 5.76 | 20 | 1 |
EBS-DM [description not available] | 0 | 13.56 | 172 | 1 |
Epidermolysis Bullosa Simplex A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex. | 0 | 13.56 | 172 | 1 |
Adhesions, Tissue [description not available] | 0 | 3.75 | 10 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 12.45 | 257 | 0 |
Innate Inflammatory Response [description not available] | 0 | 14.14 | 126 | 6 |
Endometrial Diseases [description not available] | 0 | 3.39 | 7 | 0 |
Inflammation A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function. | 0 | 14.14 | 126 | 6 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 12.68 | 474 | 2 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 3.39 | 7 | 0 |
Cancer of Colon [description not available] | 0 | 12.86 | 151 | 6 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 12.86 | 151 | 6 |
Carcinoma, Anaplastic [description not available] | 0 | 15.86 | 693 | 3 |
Cancer of Stomach [description not available] | 0 | 11.63 | 188 | 1 |
Carcinoma A malignant neoplasm made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. It is a histological type of neoplasm and not a synonym for cancer. | 0 | 15.86 | 693 | 3 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 11.63 | 188 | 1 |
Benign Neoplasms [description not available] | 0 | 15.98 | 244 | 3 |
Bone Tissue Neoplasms [description not available] | 0 | 2.31 | 1 | 0 |
Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. | 0 | 15.98 | 244 | 3 |
Colitis-Associated Cancer [description not available] | 0 | 2.41 | 1 | 0 |
Colitis Gravis [description not available] | 0 | 3.88 | 12 | 0 |
Colitis, Ulcerative Inflammation of the COLON that is predominantly confined to the MUCOSA. Its major symptoms include DIARRHEA, rectal BLEEDING, the passage of MUCUS, and ABDOMINAL PAIN. | 0 | 3.88 | 12 | 0 |
Malignant Mesothelioma [description not available] | 0 | 5.06 | 8 | 1 |
Cancer of Lung [description not available] | 0 | 19.95 | 750 | 21 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 19.95 | 750 | 21 |
Mesothelioma A tumor derived from mesothelial tissue (peritoneum, pleura, pericardium). It appears as broad sheets of cells, with some regions containing spindle-shaped, sarcoma-like cells and other regions showing adenomatous patterns. Pleural mesotheliomas have been linked to exposure to asbestos. (Dorland, 27th ed) | 0 | 12.14 | 218 | 1 |
2019 Novel Coronavirus Disease [description not available] | 0 | 4.25 | 4 | 0 |
Eye Disorders [description not available] | 0 | 4.28 | 19 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 4.28 | 19 | 0 |
Periimplantitis [description not available] | 0 | 7 | 5 | 2 |
Peri-Implantitis An inflammatory process with loss of supporting bone in the tissues surrounding functioning DENTAL IMPLANTS. | 0 | 7 | 5 | 2 |
Carcinoma, Epidermoid [description not available] | 0 | 18.38 | 1,258 | 7 |
Metastase [description not available] | 0 | 17.26 | 294 | 8 |
Cancer of Skin [description not available] | 0 | 16.06 | 921 | 3 |
Invasiveness, Neoplasm [description not available] | 0 | 15.27 | 349 | 3 |
Carcinoma, Squamous Cell A carcinoma derived from stratified SQUAMOUS EPITHELIAL CELLS. It may also occur in sites where glandular or columnar epithelium is normally present. (From Stedman, 25th ed) | 0 | 18.38 | 1,258 | 7 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 17.26 | 294 | 8 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 16.06 | 921 | 3 |
Breast Cancer [description not available] | 0 | 21.18 | 995 | 21 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 21.18 | 995 | 21 |
Anaplastic Large-Cell Lymphoma [description not available] | 0 | 4.25 | 6 | 0 |
Lymphoma, Large-Cell, Anaplastic A systemic, large-cell, non-Hodgkin, malignant lymphoma characterized by cells with pleomorphic appearance and expressing the CD30 ANTIGEN. These so-called hallmark cells have lobulated and indented nuclei. This lymphoma is often mistaken for metastatic carcinoma and MALIGNANT HISTIOCYTOSIS. | 0 | 4.25 | 6 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 4.04 | 5 | 0 |
Abnormalities, Skin [description not available] | 0 | 6.66 | 24 | 0 |
Cardiomyopathies A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS). | 0 | 4.04 | 5 | 0 |
Skin Abnormalities Congenital structural abnormalities of the skin. | 0 | 6.66 | 24 | 0 |
Dysembryoma [description not available] | 0 | 7.27 | 71 | 0 |
Teratoma A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642) | 0 | 7.27 | 71 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 16.25 | 204 | 14 |
Carcinoma, Non-Small-Cell Lung A heterogeneous aggregate of at least three distinct histological types of lung cancer, including SQUAMOUS CELL CARCINOMA; ADENOCARCINOMA; and LARGE CELL CARCINOMA. They are dealt with collectively because of their shared treatment strategy. | 0 | 16.25 | 204 | 14 |
Adenoma, Basal Cell [description not available] | 0 | 9.64 | 219 | 0 |
Cancer of Pituitary [description not available] | 0 | 7.15 | 62 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 9.64 | 219 | 0 |
Pituitary Neoplasms Neoplasms which arise from or metastasize to the PITUITARY GLAND. The majority of pituitary neoplasms are adenomas, which are divided into non-secreting and secreting forms. Hormone producing forms are further classified by the type of hormone they secrete. Pituitary adenomas may also be characterized by their staining properties (see ADENOMA, BASOPHIL; ADENOMA, ACIDOPHIL; and ADENOMA, CHROMOPHOBE). Pituitary tumors may compress adjacent structures, including the HYPOTHALAMUS, several CRANIAL NERVES, and the OPTIC CHIASM. Chiasmal compression may result in bitemporal HEMIANOPSIA. | 0 | 7.15 | 62 | 0 |
Eczema, Atopic [description not available] | 0 | 7.35 | 41 | 0 |
Dermatitis, Atopic A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. | 0 | 7.35 | 41 | 0 |
Cancer of Maxillary Sinus [description not available] | 0 | 5.55 | 16 | 0 |
Carcinoma, Neuroendocrine A group of carcinomas which share a characteristic morphology, often being composed of clusters and trabecular sheets of round blue cells, granular chromatin, and an attenuated rim of poorly demarcated cytoplasm. Neuroendocrine tumors include carcinoids, small (oat) cell carcinomas, medullary carcinoma of the thyroid, Merkel cell tumor, cutaneous neuroendocrine carcinoma, pancreatic islet cell tumors, and pheochromocytoma. Neurosecretory granules are found within the tumor cells. (Segen, Dictionary of Modern Medicine, 1992) | 0 | 8.01 | 54 | 0 |
Carcinoma, Mucoepidermoid A tumor of both low- and high-grade malignancy. The low-grade grow slowly, appear in any age group, and are readily cured by excision. The high-grade behave aggressively, widely infiltrate the salivary gland and produce lymph node and distant metastases. Mucoepidermoid carcinomas account for about 21% of the malignant tumors of the parotid gland and 10% of the sublingual gland. They are the most common malignant tumor of the parotid. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p575; Holland et al., Cancer Medicine, 3d ed, p1240) | 0 | 7.06 | 35 | 0 |
Cancer of Salivary Gland [description not available] | 0 | 9.9 | 175 | 0 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 9.9 | 175 | 0 |
Hyperkeratosis Palmaris et Plantaris [description not available] | 0 | 12.32 | 146 | 0 |
E coli Infections [description not available] | 0 | 3.06 | 4 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 3.06 | 4 | 0 |
Cystic Echinococcosis [description not available] | 0 | 2.41 | 1 | 0 |
Alveolar Echinococcosis, Hepatic [description not available] | 0 | 2.41 | 1 | 0 |
Cancer of Head [description not available] | 0 | 10.59 | 180 | 0 |
Ewing Sarcoma [description not available] | 0 | 6.92 | 30 | 0 |
Adamantinoma A locally aggressive, osteolytic neoplasm of the long bones, probably of epithelial origin and most often involving the TIBIA. | 0 | 3.98 | 12 | 0 |
Ameloblastoma An immature epithelial tumor of the JAW originating from the epithelial rests of Malassez or from other epithelial remnants of the ENAMEL from the developmental period. It is a slowly growing tumor, usually benign, but displays a marked propensity for invasive growth. | 0 | 9.61 | 100 | 0 |
Head and Neck Neoplasms Soft tissue tumors or cancer arising from the mucosal surfaces of the LIP; oral cavity; PHARYNX; LARYNX; and cervical esophagus. Other sites included are the NOSE and PARANASAL SINUSES; SALIVARY GLANDS; THYROID GLAND and PARATHYROID GLANDS; and MELANOMA and non-melanoma skin cancers of the head and neck. (from Holland et al., Cancer Medicine, 4th ed, p1651) | 0 | 10.59 | 180 | 0 |
Sarcoma, Ewing A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. The tumor occurs usually before the age of 20, about twice as frequently in males as in females. | 0 | 6.92 | 30 | 0 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 11.36 | 147 | 1 |
Paraganglioma, Gangliocytic [description not available] | 0 | 6.46 | 30 | 0 |
Peripheral Nerve Neoplasms [description not available] | 0 | 5.32 | 21 | 0 |
Paraganglioma A neural crest tumor usually derived from the chromoreceptor tissue of a paraganglion, such as the carotid body, or medulla of the adrenal gland (usually called a chromaffinoma or pheochromocytoma). It is more common in women than in men. (Stedman, 25th ed; from Segen, Dictionary of Modern Medicine, 1992) | 0 | 6.46 | 30 | 0 |
Peripheral Nervous System Neoplasms Neoplasms which arise from peripheral nerve tissue. This includes NEUROFIBROMAS; SCHWANNOMAS; GRANULAR CELL TUMORS; and malignant peripheral NERVE SHEATH NEOPLASMS. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp1750-1) | 0 | 5.32 | 21 | 0 |
Neuroendocrine Tumors Tumors whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumors include ectopic hormone production (often via APUD CELLS), the presence of tumor-associated antigens, and isozyme composition. | 0 | 6.75 | 21 | 0 |
Equine Diseases [description not available] | 0 | 8.26 | 26 | 0 |
Dental Tissue Neoplasms [description not available] | 0 | 9.48 | 113 | 0 |
Mandibular Neoplasms Tumors or cancer of the MANDIBLE. | 0 | 9.31 | 97 | 0 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 4.82 | 7 | 0 |
Epidermal Cyst Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules. | 0 | 10.15 | 117 | 0 |
Corneal Diseases Diseases of the cornea. | 0 | 8.4 | 53 | 0 |
Fibrous Tissue Neoplasms [description not available] | 0 | 2.94 | 4 | 0 |
Poultry Diseases Diseases of birds which are raised as a source of meat or eggs for human consumption and are usually found in barnyards, hatcheries, etc. The concept is differentiated from BIRD DISEASES which is for diseases of birds not considered poultry and usually found in zoos, parks, and the wild. | 0 | 2.91 | 4 | 0 |
Electrolytes Substances that dissociate into two or more ions, to some extent, in water. Solutions of electrolytes thus conduct an electric current and can be decomposed by it (ELECTROLYSIS). (Grant & Hackh's Chemical Dictionary, 5th ed) | 0 | 4.62 | 6 | 0 |
Acne Inversa [description not available] | 0 | 5.26 | 11 | 0 |
Hidradenitis Suppurativa A chronic suppurative and cicatricial disease of the apocrine glands occurring chiefly in the axillae in women and in the groin and anal regions in men. It is characterized by poral occlusion with secondary bacterial infection, evolving into abscesses which eventually rupture. As the disease becomes chronic, ulcers appear, sinus tracts enlarge, fistulas develop, and fibrosis and scarring become evident. | 0 | 5.26 | 11 | 0 |
Micrometastases, Neoplasm [description not available] | 0 | 4.17 | 15 | 0 |
Cancer of Cervix [description not available] | 0 | 12.45 | 211 | 1 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 12.45 | 211 | 1 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 4.4 | 21 | 0 |
Lymphoma, Large B-Cell, Diffuse Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation. | 0 | 4.4 | 21 | 0 |
Carcinoma, Ductal, Breast An invasive (infiltrating) CARCINOMA of the mammary ductal system (MAMMARY GLANDS) in the human BREAST. | 0 | 11.53 | 129 | 1 |
Carcinoma, Lobular A type of BREAST CANCER where the abnormal malignant cells form in the lobules, or milk-producing glands, of the breast. | 0 | 11.13 | 75 | 2 |
Solitary Fibrous Tumors Rare neoplasms of mesenchymal origin, usually benign, and most commonly involving the PLEURA (see SOLITARY FIBROUS TUMOR, PLEURAL). They also are found in extrapleural sites. | 0 | 4.41 | 7 | 0 |
Bone Cancer [description not available] | 0 | 10 | 101 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 10 | 101 | 0 |
Soft Tissue Neoplasms Neoplasms of whatever cell type or origin, occurring in the extraskeletal connective tissue framework of the body including the organs of locomotion and their various component structures, such as nerves, blood vessels, lymphatics, etc. | 0 | 8.96 | 109 | 0 |
Malignant Fibrohistiocytic Tumors [description not available] | 0 | 3.49 | 7 | 0 |
Fibrosarcoma A sarcoma derived from deep fibrous tissue, characterized by bundles of immature proliferating fibroblasts with variable collagen formation, which tends to invade locally and metastasize by the bloodstream. (Stedman, 25th ed) | 0 | 5.87 | 23 | 0 |
Osteomyelitis INFLAMMATION of the bone as a result of infection. It may be caused by a variety of infectious agents, especially pyogenic (PUS - producing) BACTERIA. | 0 | 2.53 | 2 | 0 |
Histiocytoma, Malignant Fibrous The most commonly diagnosed soft tissue sarcoma. It is a neoplasm with a fibrohistiocytic appearance found chiefly in later adult life, with peak incidence in the 7th decade. | 0 | 3.49 | 7 | 0 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 4.77 | 6 | 0 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 4.77 | 6 | 0 |
Adenoma, Pleomorphic A benign, slow-growing tumor, most commonly of the salivary gland, occurring as a small, painless, firm nodule, usually of the parotid gland, but also found in any major or accessory salivary gland anywhere in the oral cavity. It is most often seen in women in the fifth decade. Histologically, the tumor presents a variety of cells: cuboidal, columnar, and squamous cells, showing all forms of epithelial growth. (Dorland, 27th ed) | 0 | 7.83 | 80 | 0 |
Myoepithelial Tumor [description not available] | 0 | 8.25 | 78 | 0 |
Myoepithelioma A usually benign tumor made up predominantly of myoepithelial cells. | 0 | 8.25 | 78 | 0 |
Canine Diseases [description not available] | 0 | 5.99 | 105 | 0 |
Keratocysts [description not available] | 0 | 10.19 | 238 | 0 |
Dendritic Cell Sarcoma, Follicular Sarcoma of FOLLICULAR DENDRITIC CELLS most often found in the lymph nodes. This rare neoplasm occurs predominately in adults. | 0 | 2.9 | 2 | 0 |
Bladder Cancer [description not available] | 0 | 15.99 | 274 | 13 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 15.99 | 274 | 13 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 13.15 | 190 | 5 |
Neoplasm Metastasis, Unknown Primary [description not available] | 0 | 7.96 | 47 | 0 |
Palmoplantaris Pustulosis [description not available] | 0 | 15.13 | 329 | 26 |
Psoriasis A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. | 0 | 15.13 | 329 | 26 |
Alloxan Diabetes [description not available] | 0 | 4.43 | 21 | 0 |
Drug-Induced Stevens Johnson Syndrome [description not available] | 0 | 4.71 | 11 | 0 |
Stevens-Johnson Syndrome Rare cutaneous eruption characterized by extensive KERATINOCYTE apoptosis resulting in skin detachment with mucosal involvement. It is often provoked by the use of drugs (e.g., antibiotics and anticonvulsants) or associated with PNEUMONIA, MYCOPLASMA. It is considered a continuum of Toxic Epidermal Necrolysis. | 0 | 4.71 | 11 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 3.89 | 12 | 0 |
Epidermolytic Palmoplantar Keratoderma Vorner Type [description not available] | 0 | 3.12 | 4 | 0 |
Cold Panniculitis [description not available] | 0 | 2.41 | 1 | 0 |
Bullous Congenital Ichthyosiform Erythroderma [description not available] | 0 | 12.01 | 124 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 8.38 | 53 | 1 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 7.99 | 93 | 0 |
Carcinoma, Papillary A malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. (Stedman, 25th ed) | 0 | 8.98 | 133 | 0 |
Nail Diseases Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. | 0 | 7.53 | 49 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 10.2 | 95 | 1 |
Brain Neoplasms Neoplasms of the intracranial components of the central nervous system, including the cerebral hemispheres, basal ganglia, hypothalamus, thalamus, brain stem, and cerebellum. Brain neoplasms are subdivided into primary (originating from brain tissue) and secondary (i.e., metastatic) forms. Primary neoplasms are subdivided into benign and malignant forms. In general, brain tumors may also be classified by age of onset, histologic type, or presenting location in the brain. | 0 | 10.2 | 95 | 1 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 5.38 | 19 | 0 |
Squamous Cell Carcinoma of Head and Neck The most common type of head and neck carcinoma that originates from cells on the surface of the NASAL CAVITY; MOUTH; PARANASAL SINUSES, SALIVARY GLANDS, and LARYNX. Mutations in TNFRSF10B, PTEN, and ING1 genes are associated with this cancer. | 0 | 5.38 | 19 | 0 |
Chordoma A malignant tumor arising from the embryonic remains of the notochord. It is also called chordocarcinoma, chordoepithelioma, and notochordoma. (Dorland, 27th ed) | 0 | 9.99 | 77 | 0 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 8.09 | 34 | 0 |
Epithelial Neoplasms [description not available] | 0 | 8.24 | 52 | 0 |
Giant Cell Tumors Tumors of bone tissue or synovial or other soft tissue characterized by the presence of giant cells. The most common are giant cell tumor of tendon sheath and GIANT CELL TUMOR OF BONE. | 0 | 5.05 | 16 | 0 |
Jaundice, Cholestatic [description not available] | 0 | 2.79 | 3 | 0 |
Jaundice, Obstructive Jaundice, the condition with yellowish staining of the skin and mucous membranes, that is due to impaired BILE flow in the BILIARY TRACT, such as INTRAHEPATIC CHOLESTASIS, or EXTRAHEPATIC CHOLESTASIS. | 0 | 2.79 | 3 | 0 |
Injuries, Radiation [description not available] | 0 | 6.84 | 9 | 1 |
Mucositis, Oral [description not available] | 0 | 8.95 | 18 | 1 |
Stomatitis INFLAMMATION of the soft tissues of the MOUTH, such as MUCOSA; PALATE; GINGIVA; and LIP. | 0 | 8.95 | 18 | 1 |
Mucositis An INFLAMMATION of the MUCOSA with burning or tingling sensation. It is characterized by atrophy of the squamous EPITHELIUM, vascular damage, inflammatory infiltration, and ulceration. It usually occurs at the mucous lining of the MOUTH, the GASTROINTESTINAL TRACT or the airway due to chemical irritations, CHEMOTHERAPY, or radiation therapy (RADIOTHERAPY). | 0 | 4.62 | 3 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 10.62 | 172 | 1 |
Cancer of Liver [description not available] | 0 | 12.68 | 311 | 2 |
Cancer of Prostate [description not available] | 0 | 15.26 | 352 | 7 |
Carcinoma, Hepatocellular A primary malignant neoplasm of epithelial liver cells. It ranges from a well-differentiated tumor with EPITHELIAL CELLS indistinguishable from normal HEPATOCYTES to a poorly differentiated neoplasm. The cells may be uniform or markedly pleomorphic, or form GIANT CELLS. Several classification schemes have been suggested. | 0 | 10.62 | 172 | 1 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 12.68 | 311 | 2 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 15.26 | 352 | 7 |
Blastoma, Pulmonary [description not available] | 0 | 5.12 | 7 | 0 |
Rhabdomyosarcoma, Embryonal A form of RHABDOMYOSARCOMA arising primarily in the head and neck, especially the orbit, of children below the age of 10. The cells are smaller than those of other rhabdomyosarcomas and are of two basic cell types: spindle cells and round cells. This cancer is highly sensitive to chemotherapy and has a high cure rate with multi-modality therapy. (From Holland et al., Cancer Medicine, 3d ed, p2188) | 0 | 3.16 | 5 | 0 |
Keratoderma Blennorrhagicum [description not available] | 0 | 12.38 | 175 | 1 |
Keratosis Any horny growth such as a wart or callus. | 0 | 12.38 | 175 | 1 |
Adenopathy [description not available] | 0 | 3.33 | 1 | 0 |
Lymph Node Metastasis [description not available] | 0 | 18.39 | 598 | 18 |
Cancer of Mouth [description not available] | 0 | 13.12 | 303 | 1 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 13.12 | 303 | 1 |
Nail Fungus [description not available] | 0 | 5.7 | 31 | 0 |
Onychomycosis A fungal infection of the nail, usually caused by DERMATOPHYTES; YEASTS; or nondermatophyte MOLDS. | 0 | 5.7 | 31 | 0 |
Cancer of Endometrium [description not available] | 0 | 8.34 | 80 | 0 |
Endometrial Neoplasms Tumors or cancer of ENDOMETRIUM, the mucous lining of the UTERUS. These neoplasms can be benign or malignant. Their classification and grading are based on the various cell types and the percent of undifferentiated cells. | 0 | 8.34 | 80 | 0 |
Neuroectodermal Tumors Malignant neoplasms arising in the neuroectoderm, the portion of the ectoderm of the early embryo that gives rise to the central and peripheral nervous systems, including some glial cells. | 0 | 3.01 | 4 | 0 |
Bile Duct Cancer [description not available] | 0 | 7.81 | 65 | 0 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 7.81 | 65 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 5.08 | 5 | 0 |
Anoxemia [description not available] | 0 | 4.23 | 6 | 0 |
Cells, Neoplasm Circulating [description not available] | 0 | 17.55 | 252 | 11 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 4.23 | 6 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 10.31 | 138 | 1 |
Cancer of Kidney [description not available] | 0 | 11.68 | 270 | 1 |
Carcinoma, Renal Cell A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma. | 0 | 10.31 | 138 | 1 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 11.68 | 270 | 1 |
Bleeding [description not available] | 0 | 5.38 | 13 | 0 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 5.38 | 13 | 0 |
Adrenocortical Carcinoma A malignant neoplasm of the ADRENAL CORTEX. Adrenocortical carcinomas are unencapsulated anaplastic (ANAPLASIA) masses sometimes exceeding 20 cm or 200 g. They are more likely to be functional than nonfunctional, and produce ADRENAL CORTEX HORMONES that may result in hypercortisolism (CUSHING SYNDROME); HYPERALDOSTERONISM; and/or VIRILISM. | 0 | 3.02 | 4 | 0 |
Adrenal Cortex Cancer [description not available] | 0 | 5.47 | 15 | 0 |
Adrenal Cortex Neoplasms Tumors or cancers of the ADRENAL CORTEX. | 0 | 5.47 | 15 | 0 |
Carcinoma, Thymic [description not available] | 0 | 7.25 | 69 | 0 |
Cancer of the Thymus [description not available] | 0 | 8.2 | 85 | 0 |
Hyperplasia An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells. | 0 | 11.77 | 313 | 0 |
Thymoma A neoplasm originating from thymic tissue, usually benign, and frequently encapsulated. Although it is occasionally invasive, metastases are extremely rare. It consists of any type of thymic epithelial cell as well as lymphocytes that are usually abundant. Malignant lymphomas that involve the thymus, e.g., lymphosarcoma, Hodgkin's disease (previously termed granulomatous thymoma), should not be regarded as thymoma. (From Stedman, 25th ed) | 0 | 7.25 | 69 | 0 |
Thymus Neoplasms Tumors or cancer of the THYMUS GLAND. | 0 | 8.2 | 85 | 0 |
Bone Fractures [description not available] | 0 | 4.27 | 7 | 0 |
Fractures, Bone Breaks in bones. | 0 | 4.27 | 7 | 0 |
Congenital Pachyonychia [description not available] | 0 | 6.74 | 19 | 0 |
Pachyonychia Congenita A group of inherited ectodermal dysplasias whose most prominent clinical feature is hypertrophic nail dystrophy resulting in PACHYONYCHIA. Several specific subtypes of pachyonychia congenita have been associated with mutations in genes that encode KERATINS. | 0 | 6.74 | 19 | 0 |
Carcinoma, Adenosquamous A mixed adenocarcinoma and squamous cell or epidermoid carcinoma. | 0 | 7.18 | 40 | 0 |
Extracapsular Extension [description not available] | 0 | 2.41 | 1 | 0 |
Cirrhosis [description not available] | 0 | 9.48 | 48 | 1 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 9.48 | 48 | 1 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 6.58 | 27 | 0 |
Malignant Melanoma [description not available] | 0 | 11.06 | 154 | 1 |
Melanoma A malignant neoplasm derived from cells that are capable of forming melanin, which may occur in the skin of any part of the body, in the eye, or, rarely, in the mucous membranes of the genitalia, anus, oral cavity, or other sites. It occurs mostly in adults and may originate de novo or from a pigmented nevus or malignant lentigo. Melanomas frequently metastasize widely, and the regional lymph nodes, liver, lungs, and brain are likely to be involved. The incidence of malignant skin melanomas is rising rapidly in all parts of the world. (Stedman, 25th ed; from Rook et al., Textbook of Dermatology, 4th ed, p2445) | 0 | 11.06 | 154 | 1 |
Cicatrization The formation of fibrous tissue in the place of normal tissue during the process of WOUND HEALING. It includes scar tissue formation occurring in healing internal organs as well as in the skin after surface injuries. | 0 | 8.28 | 37 | 2 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 8.28 | 37 | 2 |
Astrocytoma, Grade IV [description not available] | 0 | 4.17 | 16 | 0 |
Glioblastoma A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures. | 0 | 4.17 | 16 | 0 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 2.77 | 3 | 0 |
Amyotrophic Lateral Sclerosis A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) | 0 | 2.77 | 3 | 0 |
Anal Gland Neoplasms Tumors or cancer of the anal gland. | 0 | 2.7 | 3 | 0 |
Benign Meningeal Neoplasms [description not available] | 0 | 8.53 | 48 | 1 |
Angioblastic Meningioma [description not available] | 0 | 9.35 | 59 | 1 |
Granular Cell Myoblastoma [description not available] | 0 | 5.79 | 15 | 0 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 8.53 | 48 | 1 |
Meningioma A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7) | 0 | 9.35 | 59 | 1 |
Sarcoma, Epithelioid [description not available] | 0 | 11.54 | 215 | 1 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 11.54 | 215 | 1 |
Anemia, Fanconi [description not available] | 0 | 3.34 | 2 | 0 |
Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004) | 0 | 3.34 | 2 | 0 |
Amyloid Deposits [description not available] | 0 | 2.82 | 3 | 0 |
Amyloidosis A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. | 0 | 8.18 | 44 | 1 |
Keratoconus A noninflammatory, usually bilateral protrusion of the cornea, the apex being displaced downward and nasally. It occurs most commonly in females at about puberty. The cause is unknown but hereditary factors may play a role. The -conus refers to the cone shape of the corneal protrusion. (From Dorland, 27th ed) | 0 | 4.06 | 5 | 0 |
Xeroderma [description not available] | 0 | 13.67 | 122 | 1 |
Ichthyosis Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome. | 0 | 13.67 | 122 | 1 |
ER-Negative PR-Negative HER2-Negative Breast Cancer [description not available] | 0 | 4.23 | 15 | 0 |
Triple Negative Breast Neoplasms Breast neoplasms that do not express ESTROGEN RECEPTORS; PROGESTERONE RECEPTORS; and do not overexpress the NEU RECEPTOR/HER-2 PROTO-ONCOGENE PROTEIN. | 0 | 4.23 | 15 | 0 |
Cyst [description not available] | 0 | 10.85 | 139 | 2 |
Cat Diseases Diseases of the domestic cat (Felis catus or F. domesticus). This term does not include diseases of the so-called big cats such as CHEETAHS; LIONS; tigers, cougars, panthers, leopards, and other Felidae for which the heading CARNIVORA is used. | 0 | 5.37 | 22 | 0 |
Clear Cell Sarcoma of Soft Tissue [description not available] | 0 | 5.36 | 9 | 0 |
Dysplastic Nevus Syndrome, Hereditary [description not available] | 0 | 3.01 | 3 | 0 |
Sarcoma, Clear Cell A sarcoma of young adults occurring in the lower extremities and acral regions. It is found intimately bound to tendons as a circumscribed but unencapsulated melanin-bearing tumor of neuroectodermal origin. Clear cell sarcoma is associated with a specific t(12;22)(q13;q12) translocation. | 0 | 5.36 | 9 | 0 |
Cardiac Cancer [description not available] | 0 | 5.39 | 23 | 0 |
Cancer of Mediastinum [description not available] | 0 | 5.56 | 27 | 0 |
Mediastinal Neoplasms Tumors or cancer of the MEDIASTINUM. | 0 | 5.56 | 27 | 0 |
Cancer of Parotid [description not available] | 0 | 7.68 | 83 | 0 |
Parotid Neoplasms Tumors or cancer of the PAROTID GLAND. | 0 | 7.68 | 83 | 0 |
Avian Diseases [description not available] | 0 | 3.73 | 10 | 0 |
Fasciitis Inflammation of the fascia. There are three major types: 1, Eosinophilic fasciitis, an inflammatory reaction with eosinophilia, producing hard thickened skin with an orange-peel configuration suggestive of scleroderma and considered by some a variant of scleroderma; 2, Necrotizing fasciitis (FASCIITIS, NECROTIZING), a serious fulminating infection (usually by a beta hemolytic streptococcus) causing extensive necrosis of superficial fascia; 3, Nodular/Pseudosarcomatous /Proliferative fasciitis, characterized by a rapid growth of fibroblasts with mononuclear inflammatory cells and proliferating capillaries in soft tissue, often the forearm; it is not malignant but is sometimes mistaken for fibrosarcoma. | 0 | 4.11 | 10 | 0 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 10.51 | 209 | 0 |
Carcinoma, Basal Cell A malignant skin neoplasm that seldom metastasizes but has potentialities for local invasion and destruction. Clinically it is divided into types: nodular, cicatricial, morphaic, and erythematoid (pagetoid). They develop on hair-bearing skin, most commonly on sun-exposed areas. Approximately 85% are found on the head and neck area and the remaining 15% on the trunk and limbs. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1471) | 0 | 10.51 | 209 | 0 |
Cancer of Spleen [description not available] | 0 | 6 | 14 | 0 |
Histiocytic Disorders, Malignant Distinctive neoplastic disorders of histiocytes. Included are malignant neoplasms of MACROPHAGES and DENDRITIC CELLS. | 0 | 5.59 | 5 | 0 |
Bronchiolitis, Exudative [description not available] | 0 | 3.52 | 4 | 0 |
Bronchiolitis Obliterans Inflammation of the BRONCHIOLES leading to an obstructive lung disease. Bronchioles are characterized by fibrous granulation tissue with bronchial exudates in the lumens. Clinical features include a nonproductive cough and DYSPNEA. | 0 | 3.52 | 4 | 0 |
Chemodectoma [description not available] | 0 | 2.78 | 3 | 0 |
Bleb [description not available] | 0 | 6.97 | 28 | 0 |
Pemphigus Foliaceus [description not available] | 0 | 7.48 | 56 | 0 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 7.48 | 56 | 0 |
Collodion Baby Syndrome [description not available] | 0 | 7.1 | 14 | 1 |
Ichthyosis, Lamellar A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds within a few weeks. Scaling is generalized and marked with grayish-brown quadrilateral scales, adherent at their centers and free at the edges. In some cases, scales are so thick that they resemble armored plate. | 0 | 7.1 | 14 | 1 |
Exanthem [description not available] | 0 | 2.46 | 2 | 0 |
Keratosis, Oral [description not available] | 0 | 10.21 | 88 | 1 |
Exanthema Diseases in which skin eruptions or rashes are a prominent manifestation. Classically, six such diseases were described with similar rashes; they were numbered in the order in which they were reported. Only the fourth (Duke's disease), fifth (ERYTHEMA INFECTIOSUM), and sixth (EXANTHEMA SUBITUM) numeric designations survive as occasional synonyms in current terminology. | 0 | 2.46 | 2 | 0 |
Leukoplakia, Oral A white patch seen on the oral mucosa. It is considered a premalignant condition and is often tobacco-induced. When evidence of Epstein-Barr virus is present, the condition is called hairy leukoplakia (LEUKOPLAKIA, HAIRY). | 0 | 10.21 | 88 | 1 |
Mange, Sarcoptic [description not available] | 0 | 3 | 4 | 0 |
Scabies A contagious cutaneous inflammation caused by the bite of the mite SARCOPTES SCABIEI. It is characterized by pruritic papular eruptions and burrows and affects primarily the axillae, elbows, wrists, and genitalia, although it can spread to cover the entire body. | 0 | 3 | 4 | 0 |
Chondrosarcoma A slowly growing malignant neoplasm derived from cartilage cells, occurring most frequently in pelvic bones or near the ends of long bones, in middle-aged and old people. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion or in patients with ENCHONDROMATOSIS. (Stedman, 25th ed) | 0 | 8.99 | 41 | 0 |
Liver Dysfunction [description not available] | 0 | 9.18 | 80 | 0 |
Liver Diseases Pathological processes of the LIVER. | 0 | 9.18 | 80 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 11.19 | 122 | 1 |
Cancer of the Vulva [description not available] | 0 | 8.64 | 61 | 0 |
Carcinoma in Situ A lesion with cytological characteristics associated with invasive carcinoma but the tumor cells are confined to the epithelium of origin, without invasion of the basement membrane. | 0 | 11.19 | 122 | 1 |
Vulvar Neoplasms Tumors or cancer of the VULVA. | 0 | 8.64 | 61 | 0 |
Dental Plaque A film that attaches to teeth, often causing DENTAL CARIES and GINGIVITIS. It is composed of MUCINS, secreted from salivary glands, and microorganisms. | 0 | 10.41 | 27 | 4 |
Carcinoma, Small Cell Lung [description not available] | 0 | 3.97 | 12 | 0 |
Small Cell Lung Carcinoma A form of highly malignant lung cancer that is composed of small ovoid cells (SMALL CELL CARCINOMA). | 0 | 3.97 | 12 | 0 |
Cicatrix, Hypertrophic An elevated scar, resembling a KELOID, but which does not spread into surrounding tissues. It is formed by enlargement and overgrowth of cicatricial tissue and regresses spontaneously. | 0 | 5.12 | 10 | 1 |
Esophageal Diseases Pathological processes in the ESOPHAGUS. | 0 | 4.72 | 11 | 0 |
Aesthesioneuroblastoma [description not available] | 0 | 5.33 | 8 | 0 |
Cancer of Nose [description not available] | 0 | 7.42 | 52 | 0 |
Cancer of Paranasal Sinus [description not available] | 0 | 7.03 | 35 | 0 |
Paranasal Sinus Neoplasms Tumors or cancer of the PARANASAL SINUSES. | 0 | 7.03 | 35 | 0 |
Esthesioneuroblastoma, Olfactory A malignant olfactory neuroblastoma arising from the olfactory epithelium of the superior nasal cavity and cribriform plate. It is uncommon (3% of nasal tumors) and rarely is associated with the production of excess hormones (e.g., SIADH, Cushing Syndrome). It has a high propensity for multiple local recurrences and bony metastases. (From Holland et al., Cancer Medicine, 3rd ed, p1245; J Laryngol Otol 1998 Jul;112(7):628-33) | 0 | 5.33 | 8 | 0 |
Local Neoplasm Recurrence [description not available] | 0 | 16.34 | 296 | 5 |
Arthritis, Degenerative [description not available] | 0 | 4.46 | 5 | 0 |
Osteoarthritis A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans. | 0 | 4.46 | 5 | 0 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 2.39 | 2 | 0 |
Aqueductal Stenosis [description not available] | 0 | 3.24 | 6 | 0 |
Pericementitis [description not available] | 0 | 6.3 | 23 | 0 |
Alveolar Bone Atrophy [description not available] | 0 | 10.18 | 23 | 4 |
Periodontitis Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology) | 0 | 6.3 | 23 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 3.23 | 5 | 0 |
Leukemia, Myeloid, Acute Clonal expansion of myeloid blasts in bone marrow, blood, and other tissue. Myeloid leukemias develop from changes in cells that normally produce NEUTROPHILS; BASOPHILS; EOSINOPHILS; and MONOCYTES. | 0 | 3.23 | 5 | 0 |
Adenocarcinoma, Clear Cell An adenocarcinoma characterized by the presence of varying combinations of clear and hobnail-shaped tumor cells. There are three predominant patterns described as tubulocystic, solid, and papillary. These tumors, usually located in the female reproductive organs, have been seen more frequently in young women since 1970 as a result of the association with intrauterine exposure to diethylstilbestrol. (From Holland et al., Cancer Medicine, 3d ed) | 0 | 8.16 | 52 | 0 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 9.03 | 71 | 0 |
Xanthoma [description not available] | 0 | 5.55 | 16 | 0 |
Parakeratosis Persistence of the nuclei of the keratinocytes into the stratum corneum of the skin. This is a normal state only in the epithelium of true mucous membranes in the mouth and vagina. (Dorland, 27th ed) | 0 | 4.78 | 32 | 0 |
Anal Cancer [description not available] | 0 | 5.95 | 25 | 0 |
Bowen Disease [description not available] | 0 | 6.54 | 29 | 0 |
Anus Neoplasms Tumors or cancer of the ANAL CANAL. | 0 | 5.95 | 25 | 0 |
Infections, Staphylococcal [description not available] | 0 | 5.38 | 14 | 1 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 5.38 | 14 | 1 |
Granulomas [description not available] | 0 | 5.89 | 39 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 5.89 | 39 | 0 |
Actinic Keratosis [description not available] | 0 | 3.04 | 5 | 0 |
Lentigines [description not available] | 0 | 4.03 | 5 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 5.49 | 26 | 0 |
Freckle, Melanotic [description not available] | 0 | 2.47 | 2 | 0 |
Lentigo Small circumscribed melanoses resembling, but differing histologically from, freckles. The concept includes senile lentigo ('liver spots') and nevoid lentigo (nevus spilus, lentigo simplex) and may also occur in association with multiple congenital defects or congenital syndromes (e.g., Peutz-Jeghers syndrome). | 0 | 4.03 | 5 | 0 |
Keratosis, Actinic White or pink lesions on the arms, hands, face, or scalp that arise from sun-induced DNA DAMAGE to KERATINOCYTES in exposed areas. They are considered precursor lesions to superficial SQUAMOUS CELL CARCINOMA. | 0 | 3.04 | 5 | 0 |
Tooth Loss The failure to retain teeth as a result of disease or injury. | 0 | 2.5 | 2 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 8.71 | 74 | 1 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 8.71 | 74 | 1 |
6th Nerve Palsy [description not available] | 0 | 2.25 | 1 | 0 |
Itching [description not available] | 0 | 3.51 | 8 | 0 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 0 | 3.51 | 8 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 5.33 | 56 | 0 |
Focal Epithelial Hyperplasia Hyperplasia of the mucous membrane of the lips, tongue, and less commonly, the buccal mucosa, floor of the mouth, and palate, presenting soft, painless, round to oval sessile papules about 1 to 4 mm in diameter. The condition usually occurs in children and young adults and has familial predilection, lasting for several months, sometimes years, before running its course. A viral etiology is suspected, the isolated organism being usually the human papillomavirus. (Jablonski, Illustrated Dictionary of Dentistry; Belshe, Textbook of Human Virology, 2d ed, p954) | 0 | 2.74 | 3 | 0 |
HPV Infection [description not available] | 0 | 6.6 | 30 | 0 |
Genital Warts [description not available] | 0 | 5.24 | 20 | 0 |
Mole, Skin [description not available] | 0 | 9.83 | 37 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 8.88 | 136 | 0 |
Hereditary Mucosal Leukokeratosis [description not available] | 0 | 2.21 | 1 | 0 |
Condylomata Acuminata Sexually transmitted form of anogenital warty growth caused by the human papillomaviruses. | 0 | 5.24 | 20 | 0 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 8.88 | 136 | 0 |
Papillomavirus Infections Neoplasms of the skin and mucous membranes caused by papillomaviruses. They are usually benign but some have a high risk for malignant progression. | 0 | 6.6 | 30 | 0 |
Glial Cell Tumors [description not available] | 0 | 6.52 | 21 | 0 |
Glioma Benign and malignant central nervous system neoplasms derived from glial cells (i.e., astrocytes, oligodendrocytes, and ependymocytes). Astrocytes may give rise to astrocytomas (ASTROCYTOMA) or glioblastoma multiforme (see GLIOBLASTOMA). Oligodendrocytes give rise to oligodendrogliomas (OLIGODENDROGLIOMA) and ependymocytes may undergo transformation to become EPENDYMOMA; CHOROID PLEXUS NEOPLASMS; or colloid cysts of the third ventricle. (From Escourolle et al., Manual of Basic Neuropathology, 2nd ed, p21) | 0 | 6.52 | 21 | 0 |
Pachymeningitis [description not available] | 0 | 3.2 | 6 | 0 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 2.91 | 4 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 2.9 | 4 | 0 |
Meningitis Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacterial, and fungal) are the most common causes of this condition, but subarachnoid hemorrhage (HEMORRHAGES, SUBARACHNOID), chemical irritation (chemical MENINGITIS), granulomatous conditions, neoplastic conditions (CARCINOMATOUS MENINGITIS), and other inflammatory conditions may produce this syndrome. (From Joynt, Clinical Neurology, 1994, Ch24, p6) | 0 | 3.2 | 6 | 0 |
Neoplasms, Squamous Cell Neoplasms of the SQUAMOUS EPITHELIAL CELLS. The concept does not refer to neoplasms located in tissue composed of squamous elements. | 0 | 3.64 | 9 | 0 |
Cancer of Muscle [description not available] | 0 | 2.21 | 1 | 0 |
Cancer of the Thyroid [description not available] | 0 | 10.89 | 164 | 1 |
Carcinosarcoma A malignant neoplasm that contains elements of carcinoma and sarcoma so extensively intermixed as to indicate neoplasia of epithelial and mesenchymal tissue. (Stedman, 25th ed) | 0 | 8.99 | 98 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 10.89 | 164 | 1 |
Cell Transformation, Neoplastic Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill. | 0 | 13.65 | 410 | 1 |
Cheilitis Inflammation of the lips. It is of various etiologies and degrees of pathology. | 0 | 5.69 | 7 | 1 |
Hair Diseases Diseases affecting the orderly growth and persistence of hair. | 0 | 10.89 | 93 | 2 |
Cornea Injuries [description not available] | 0 | 5.39 | 14 | 0 |
Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | 0 | 5.39 | 14 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 8.53 | 34 | 1 |
Experimental Radiation Injuries [description not available] | 0 | 3.29 | 6 | 0 |
Androgenization [description not available] | 0 | 3.12 | 5 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 4.3 | 7 | 0 |
Margins of Excision The edges of tissue removed in a surgery for assessment of the effectiveness of a surgical procedure in achieving the local control of a neoplasm and the adequacy of tumor removal. When the margin is negative or not involved by tumor (e.g., CANCER) it suggests all of the tumor has been removed by the surgery. | 0 | 3.31 | 5 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 8.59 | 51 | 1 |
Bone Loss, Osteoclastic [description not available] | 0 | 5.83 | 16 | 0 |
Aural Cholesteatoma [description not available] | 0 | 5.64 | 29 | 0 |
Cancer of Pancreas [description not available] | 0 | 13.91 | 189 | 1 |
Carcinoma, Ductal, Pancreatic [description not available] | 0 | 5.67 | 29 | 0 |
Pancreatic Neoplasms Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA). | 0 | 13.91 | 189 | 1 |
Carcinoma, Pancreatic Ductal Carcinoma that arises from the PANCREATIC DUCTS. It accounts for the majority of cancers derived from the PANCREAS. | 0 | 5.67 | 29 | 0 |
Peritoneal Carcinomatosis [description not available] | 0 | 9.4 | 90 | 0 |
Adenosarcoma A malignant neoplasm arising simultaneously or consecutively in mesodermal tissue and glandular epithelium of the same part. (Stedman, 25th ed) | 0 | 2.59 | 2 | 0 |
Peritoneal Neoplasms Tumors or cancer of the PERITONEUM. | 0 | 9.4 | 90 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 5.04 | 41 | 0 |
Follicular Cyst Cyst due to the occlusion of the duct of a follicle or small gland. | 0 | 4.72 | 11 | 0 |
Cirrhosis, Liver [description not available] | 0 | 6.47 | 42 | 1 |
Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. | 0 | 6.47 | 42 | 1 |
Complex and Mixed Neoplasms [description not available] | 0 | 3.84 | 11 | 0 |
Merkel Cell Cancer [description not available] | 0 | 7.58 | 52 | 0 |
Carcinoma, Merkel Cell A carcinoma arising from MERKEL CELLS located in the basal layer of the epidermis and occurring most commonly as a primary neuroendocrine carcinoma of the skin. Merkel cells are tactile cells of neuroectodermal origin and histologically show neurosecretory granules. The skin of the head and neck are a common site of Merkel cell carcinoma, occurring generally in elderly patients. (Holland et al., Cancer Medicine, 3d ed, p1245) | 0 | 7.58 | 52 | 0 |
Neoplasms, Complex and Mixed Neoplasms composed of more than one type of neoplastic tissue. | 0 | 3.84 | 11 | 0 |
Acanthoma A neoplasm composed of squamous or epidermal cells. | 0 | 3.33 | 6 | 0 |
Bullous Type of Ichthyosis [description not available] | 0 | 3.43 | 2 | 0 |
Alcohol Abuse [description not available] | 0 | 3.71 | 10 | 0 |
Alcoholism A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4) | 0 | 3.71 | 10 | 0 |
Ductal Carcinoma [description not available] | 0 | 5.45 | 14 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 4.98 | 38 | 0 |
Carcinoma, Ductal Malignant neoplasms involving the ductal systems of any of a number of organs, such as the MAMMARY GLANDS, the PANCREAS, the PROSTATE, or the LACRIMAL GLAND. | 0 | 5.45 | 14 | 0 |
Adenocarcinoma, Endometrioid [description not available] | 0 | 6.62 | 35 | 0 |
Hemorrhage, Uterine [description not available] | 0 | 4.32 | 7 | 0 |
Uterine Hemorrhage Bleeding from blood vessels in the UTERUS, sometimes manifested as vaginal bleeding. | 0 | 4.32 | 7 | 0 |
Carcinoma, Endometrioid An adenocarcinoma characterized by the presence of cells resembling the glandular cells of the ENDOMETRIUM. It is a common histological type of ovarian CARCINOMA and ENDOMETRIAL CARCINOMA. There is a high frequency of co-occurrence of this form of adenocarcinoma in both tissues. | 0 | 6.62 | 35 | 0 |
Hematochezia The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea. | 0 | 3.46 | 2 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 5.25 | 12 | 0 |
Colonic Polyps Discrete tissue masses that protrude into the lumen of the COLON. These POLYPS are connected to the wall of the colon either by a stalk, pedunculus, or by a broad base. | 0 | 4.04 | 5 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 3.46 | 2 | 0 |
Lymphoma, Non-Hodgkin Any of a group of malignant tumors of lymphoid tissue that differ from HODGKIN DISEASE, being more heterogeneous with respect to malignant cell lineage, clinical course, prognosis, and therapy. The only common feature among these tumors is the absence of giant REED-STERNBERG CELLS, a characteristic of Hodgkin's disease. | 0 | 5.25 | 12 | 0 |
Lung Adenocarcinoma [description not available] | 0 | 3.05 | 4 | 0 |
Adenocarcinoma of Lung A carcinoma originating in the lung and the most common lung cancer type in never-smokers. Malignant cells exhibit distinct features such as glandular epithelial, or tubular morphology. Mutations in KRAS, EGFR, BRAF, and ERBB2 genes are associated with this cancer. | 0 | 3.05 | 4 | 0 |
Chicken Pox [description not available] | 0 | 2.25 | 1 | 0 |
Shingles [description not available] | 0 | 2.93 | 4 | 0 |
Congenital Varicella Syndrome [description not available] | 0 | 2.25 | 1 | 0 |
Chickenpox A highly contagious infectious disease caused by the varicella-zoster virus (HERPESVIRUS 3, HUMAN). It usually affects children, is spread by direct contact or respiratory route via droplet nuclei, and is characterized by the appearance on the skin and mucous membranes of successive crops of typical pruritic vesicular lesions that are easily broken and become scabbed. Chickenpox is relatively benign in children, but may be complicated by pneumonia and encephalitis in adults. (From Dorland, 27th ed) | 0 | 2.25 | 1 | 0 |
Herpes Zoster An acute infectious, usually self-limited, disease believed to represent activation of latent varicella-zoster virus (HERPESVIRUS 3, HUMAN) in those who have been rendered partially immune after a previous attack of CHICKENPOX. It involves the SENSORY GANGLIA and their areas of innervation and is characterized by severe neuralgic pain along the distribution of the affected nerve and crops of clustered vesicles over the area. (From Dorland, 27th ed) | 0 | 2.93 | 4 | 0 |
Chloroma [description not available] | 0 | 3.99 | 4 | 0 |
Sarcoma, Myeloid An extramedullary tumor of immature MYELOID CELLS or MYELOBLASTS. Granulocytic sarcoma usually occurs with or follows the onset of ACUTE MYELOID LEUKEMIA. | 0 | 3.99 | 4 | 0 |
Endometrioma An enlarged area of ENDOMETRIOSIS that resembles a tumor. It is usually found in the OVARY. When it is filled with old blood, it is known as a chocolate cyst. | 0 | 5.94 | 40 | 0 |
Ache [description not available] | 0 | 5.58 | 10 | 0 |
Endometriosis A condition in which functional endometrial tissue is present outside the UTERUS. It is often confined to the PELVIS involving the OVARY, the ligaments, cul-de-sac, and the uterovesical peritoneum. | 0 | 5.94 | 40 | 0 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 5.58 | 10 | 0 |
Carcinoma, Giant Cell An epithelial neoplasm characterized by unusually large anaplastic cells. It is highly malignant with fulminant clinical course, bizarre histologic appearance and poor prognosis. It is most common in the lung and thyroid. (From Stedman, 25th ed & Segen, Dictionary of Modern Medicine, 1992) | 0 | 4.73 | 11 | 0 |
Calcification, Pathologic [description not available] | 0 | 6.6 | 50 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 6.6 | 50 | 0 |
Atypical Lipoma [description not available] | 0 | 4.73 | 11 | 0 |
Neoplasms, Skull [description not available] | 0 | 4.85 | 13 | 0 |
Lipoma A benign tumor composed of fat cells (ADIPOCYTES). It can be surrounded by a thin layer of connective tissue (encapsulated), or diffuse without the capsule. | 0 | 4.73 | 11 | 0 |
Dermatomycoses Superficial infections of the skin or its appendages by any of various fungi. | 0 | 6.1 | 30 | 0 |
Signet Ring Cell Carcinoma [description not available] | 0 | 6.91 | 37 | 0 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 5 | 15 | 0 |
Carcinoma, Signet Ring Cell A poorly differentiated adenocarcinoma in which the nucleus is pressed to one side by a cytoplasmic droplet of mucus. It usually arises in the gastrointestinal system. | 0 | 6.91 | 37 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 3.65 | 3 | 0 |
Neurodegenerative Diseases Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures. | 0 | 3.65 | 3 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 5.18 | 18 | 0 |
Chalazia [description not available] | 0 | 2.55 | 2 | 0 |
Eyelid Diseases Diseases involving the EYELIDS. | 0 | 5.81 | 21 | 0 |
Chalazion A non-neoplastic cyst of the MEIBOMIAN GLANDS of the eyelid. | 0 | 2.55 | 2 | 0 |
Dermatophytoses [description not available] | 0 | 6.63 | 37 | 0 |
Athlete's Foot [description not available] | 0 | 3.23 | 6 | 0 |
Tinea Fungal infection of keratinized tissues such as hair, skin and nails. The main causative fungi include MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON. | 0 | 6.63 | 37 | 0 |
Tinea Pedis Dermatological pruritic lesion in the feet, caused by Trichophyton rubrum, T. mentagrophytes, or Epidermophyton floccosum. | 0 | 3.23 | 6 | 0 |
Nasopharyngeal Carcinoma A carcinoma that originates in the EPITHELIUM of the NASOPHARYNX and includes four subtypes: keratinizing squamous cell, non-keratinizing, basaloid squamous cell, and PAPILLARY ADENOCARCINOMA. It is most prevalent in Southeast Asian populations and is associated with EPSTEIN-BARR VIRUS INFECTIONS. Somatic mutations associated with this cancer have been identified in NPCR, BAP1, UBAP1, ERBB2, ERBB3, MLL2, PIK3CA, KRAS, NRAS, and ARID1A genes. | 0 | 4.62 | 5 | 0 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 2.25 | 1 | 0 |
Colicky Pain [description not available] | 0 | 4.45 | 8 | 0 |
Constipation Infrequent or difficult evacuation of FECES. These symptoms are associated with a variety of causes, including low DIETARY FIBER intake, emotional or nervous disturbances, systemic and structural disorders, drug-induced aggravation, and infections. | 0 | 2.25 | 1 | 0 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 4.45 | 8 | 0 |
Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) | 0 | 5.63 | 13 | 0 |
Amniotic Fluid Embolism [description not available] | 0 | 2.71 | 3 | 0 |
Hormone-Dependent Neoplasms [description not available] | 0 | 7.12 | 23 | 0 |
Genetic Predisposition [description not available] | 0 | 9.09 | 49 | 1 |
Alopecia Circumscripta [description not available] | 0 | 5.08 | 10 | 0 |
Autoimmune Disease [description not available] | 0 | 7.42 | 34 | 0 |
Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | 0 | 5.08 | 10 | 0 |
Autoimmune Diseases Disorders that are characterized by the production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides. | 0 | 7.42 | 34 | 0 |
Adenocystic Carcinoma [description not available] | 0 | 8.18 | 74 | 0 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 7.4 | 52 | 0 |
Carcinoma, Adenoid Cystic Carcinoma characterized by bands or cylinders of hyalinized or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. When the cylinders occur within masses of epithelial cells, they give the tissue a perforated, sievelike, or cribriform appearance. Such tumors occur in the mammary glands, the mucous glands of the upper and lower respiratory tract, and the salivary glands. They are malignant but slow-growing, and tend to spread locally via the nerves. (Dorland, 27th ed) | 0 | 8.18 | 74 | 0 |
Hypermelanosis [description not available] | 0 | 3.52 | 8 | 0 |
Extra-Mammary Paget Disease [description not available] | 0 | 7.09 | 59 | 0 |
Paget Disease, Extramammary A rare cutaneous neoplasm that occurs in the elderly. It develops more frequently in women and predominantly involves apocrine gland-bearing areas, especially the vulva, scrotum, and perianal areas. The lesions develop as erythematous scaly patches that progress to crusted, pruritic, erythematous plaques. The clinical differential diagnosis includes squamous cell carcinoma in situ and superficial fungal infection. It is generally thought to be an adenocarcinoma of the epidermis, from which it extends into the contiguous epithelium of hair follicles and eccrine sweat ducts. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1478) | 0 | 7.09 | 59 | 0 |
Hyperpigmentation Excessive pigmentation of the skin, usually as a result of increased epidermal or dermal melanin pigmentation, hypermelanosis. Hyperpigmentation can be localized or generalized. The condition may arise from exposure to light, chemicals or other substances, or from a primary metabolic imbalance. | 0 | 3.52 | 8 | 0 |
Allergic Contact Dermatitis [description not available] | 0 | 3.5 | 8 | 0 |
Dermatitis, Allergic Contact A contact dermatitis due to allergic sensitization to various substances. These substances subsequently produce inflammatory reactions in the skin of those who have acquired hypersensitivity to them as a result of prior exposure. | 0 | 3.5 | 8 | 0 |
Acantholysis Separation of the prickle cells of the stratum spinosum of the epidermis, resulting in atrophy of the prickle cell layer. It is seen in diseases such as pemphigus vulgaris (see PEMPHIGUS) and DARIER DISEASE. | 0 | 4.72 | 30 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 6.09 | 11 | 1 |
Thyroid Cancer, Anaplastic [description not available] | 0 | 2.25 | 1 | 0 |
Thyroid Carcinoma, Anaplastic An aggressive THYROID GLAND malignancy which generally occurs in IODINE-deficient areas in people with previous thyroid pathology such as GOITER. It is associated with CELL DEDIFFERENTIATION of THYROID CARCINOMA (e.g., FOLLICULAR THYROID CARCINOMA; PAPILLARY THYROID CANCER). Typical initial presentation is a rapidly growing neck mass which upon metastasis is associated with DYSPHAGIA; NECK PAIN; bone pain; DYSPNEA; and NEUROLOGIC DEFICITS. | 0 | 2.25 | 1 | 0 |
Auricular Cancer [description not available] | 0 | 4.52 | 24 | 0 |
Multiple Primary Neoplasms [description not available] | 0 | 9.38 | 127 | 0 |
Ear Neoplasms Tumors or cancer of any part of the hearing and equilibrium system of the body (the EXTERNAL EAR, the MIDDLE EAR, and the INNER EAR). | 0 | 4.52 | 24 | 0 |
Skin Aging The process of aging due to changes in the structure and elasticity of the skin over time. It may be a part of physiological aging or it may be due to the effects of ultraviolet radiation, usually through exposure to sunlight. | 0 | 9.52 | 29 | 6 |
Cancer of Ovary [description not available] | 0 | 10.28 | 256 | 0 |
Ovarian Neoplasms Tumors or cancer of the OVARY. These neoplasms can be benign or malignant. They are classified according to the tissue of origin, such as the surface EPITHELIUM, the stromal endocrine cells, and the totipotent GERM CELLS. | 0 | 10.28 | 256 | 0 |
Gingivitis Inflammation of gum tissue (GINGIVA) without loss of connective tissue. | 0 | 10.23 | 51 | 2 |
Adenolymphoma A benign tumor characterized histologically by tall columnar epithelium within a lymphoid tissue stroma. It is usually found in the salivary glands, especially the parotid. | 0 | 5.9 | 24 | 0 |
Angiosarcoma [description not available] | 0 | 6.62 | 50 | 0 |
Hemangiosarcoma A rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. (Stedman, 25th ed) | 0 | 6.62 | 50 | 0 |
Hemangioendothelioma, Epithelioid A tumor of medium-to-large veins, composed of plump-to-spindled endothelial cells that bulge into vascular spaces in a tombstone-like fashion. These tumors are thought to have borderline aggression, where one-third develop local recurrences, but only rarely metastasize. It is unclear whether the epithelioid hemangioendothelioma is truly neoplastic or an exuberant tissue reaction, nor is it clear if this is equivalent to Kimura's disease (see ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA). (Segen, Dictionary of Modern Medicine, 1992) | 0 | 5.04 | 9 | 0 |
Aberrant Tissue [description not available] | 0 | 7.78 | 48 | 0 |
Cancer of the Retina [description not available] | 0 | 3.14 | 5 | 0 |
Cancer of Eye [description not available] | 0 | 7.3 | 24 | 1 |
Iris Neoplasms Tumors of the iris characterized by increased pigmentation of melanocytes. Iris nevi are composed of proliferated melanocytes and are associated with neurofibromatosis and malignant melanoma of the choroid and ciliary body. Malignant melanoma of the iris often originates from preexisting nevi. | 0 | 3.11 | 5 | 0 |
Uveal Neoplasms Tumors or cancer of the UVEA. | 0 | 4.53 | 9 | 0 |
Fungal Diseases [description not available] | 0 | 3.68 | 10 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 3.68 | 10 | 0 |
Odontogenic Cyst, Calcifying A mixed radiolucent-radiopaque lesion of the jaws with features of both a cyst and a solid neoplasm. It is characterized microscopically by an epithelial lining showing a palisaded layer of columnar basal cells, presence of ghost cell keratinization, dentinoid, and calcification. (Stedman, 25th ed) | 0 | 5.33 | 21 | 0 |
Acromegaly Due To Pituitary Adenoma [description not available] | 0 | 3.01 | 4 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 3.34 | 6 | 0 |
Acromegaly A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80) | 0 | 3.34 | 6 | 0 |
Skin Diseases, Viral Skin diseases caused by viruses. | 0 | 3.63 | 3 | 0 |
Diathesis [description not available] | 0 | 5.9 | 15 | 0 |
Bovine Diseases [description not available] | 0 | 5.74 | 33 | 0 |
Fungus Poisoning [description not available] | 0 | 2.25 | 1 | 0 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 2.69 | 2 | 0 |
Idiopathic Pulmonary Fibrosis A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. | 0 | 2.69 | 2 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 8.87 | 90 | 0 |
Carcinoma, Intraductal, Noninfiltrating A noninvasive (noninfiltrating) carcinoma of the breast characterized by a proliferation of malignant epithelial cells confined to the mammary ducts or lobules, without light-microscopy evidence of invasion through the basement membrane into the surrounding stroma. | 0 | 8.87 | 90 | 0 |
Plasmablastic Diffuse Large B-cell Lymphoma [description not available] | 0 | 2.31 | 1 | 0 |
Cancer of Duodenum [description not available] | 0 | 6.32 | 14 | 0 |
Common Bile Duct Neoplasms Tumor or cancer of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | 0 | 6.99 | 20 | 0 |
Osteoarthritis of Knee [description not available] | 0 | 4.49 | 2 | 2 |
Osteoarthritis, Knee Noninflammatory degenerative disease of the knee joint consisting of three large categories: conditions that block normal synchronous movement, conditions that produce abnormal pathways of motion, and conditions that cause stress concentration resulting in changes to articular cartilage. (Crenshaw, Campbell's Operative Orthopaedics, 8th ed, p2019) | 0 | 4.49 | 2 | 2 |
Fibromatosis [description not available] | 0 | 7.37 | 61 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 7.37 | 61 | 0 |
Cancer of Rectum [description not available] | 0 | 8.47 | 45 | 2 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 8.47 | 45 | 2 |
Nasal Polyps Focal accumulations of EDEMA fluid in the NASAL MUCOSA accompanied by HYPERPLASIA of the associated submucosal connective tissue. Polyps may be NEOPLASMS, foci of INFLAMMATION, degenerative lesions, or malformations. | 0 | 4.01 | 14 | 0 |
Keratoderma, Palmoplantar, Diffuse An autosomal dominant disorder characterized by a widely distributed, well-demarcated hyperkeratosis of the palms and soles. There is more than one genotypically distinct form, each of which is clinically similar but histologically distinguishable. Diffuse palmoplantar keratoderma is distinct from palmoplantar keratoderma (KERATODERMA, PALMOPLANTAR), as the former exhibits autosomal dominant inheritance and hyperhidrosis is frequently present. | 0 | 6.15 | 17 | 0 |
Leucocythaemia [description not available] | 0 | 5.69 | 7 | 1 |
Cancer, Second Primary [description not available] | 0 | 6.85 | 45 | 0 |
Leukemia A progressive, malignant disease of the blood-forming organs, characterized by distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemias were originally termed acute or chronic based on life expectancy but now are classified according to cellular maturity. Acute leukemias consist of predominately immature cells; chronic leukemias are composed of more mature cells. (From The Merck Manual, 2006) | 0 | 5.69 | 7 | 1 |
Carcinogenesis The origin, production or development of cancer through genotypic and phenotypic changes which upset the normal balance between cell proliferation and cell death. Carcinogenesis generally requires a constellation of steps, which may occur quickly or over a period of many years. | 0 | 4.84 | 11 | 0 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 5.28 | 12 | 0 |
Hepatitis C INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown. | 0 | 5.28 | 12 | 0 |
Mammary Analogue Secretory Carcinoma A malignant neoplasm of epithelial cells of the SALIVARY GLANDS, with microcystic architecture, low-grade nuclei, and granular vacuolated cytoplasm. | 0 | 2.31 | 1 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 11.13 | 241 | 0 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 3.4 | 2 | 0 |
Pleural Effusion, Malignant Presence of fluid in the PLEURAL CAVITY as a complication of malignant disease. Malignant pleural effusions often contain actual malignant cells. | 0 | 7.64 | 34 | 1 |
Nail Abnormalities [description not available] | 0 | 8.45 | 38 | 0 |
Cancer of the Uterus [description not available] | 0 | 8.48 | 114 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 8.48 | 114 | 0 |
Favus [description not available] | 0 | 2.39 | 2 | 0 |
Buruli Ulcer Disease [description not available] | 0 | 2.31 | 1 | 0 |
Buruli Ulcer A lesion in the skin and subcutaneous tissues due to infections by MYCOBACTERIUM ULCERANS. It was first reported in Uganda, Africa. | 0 | 2.31 | 1 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 5.6 | 29 | 0 |
Benign Pilomatricoma [description not available] | 0 | 5.25 | 19 | 0 |
Craniopharyngioma A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical) craniopharyngioma and papillary craniopharyngioma. The adamantinous form presents in children and adolescents as an expanding cystic lesion in the pituitary region. The cystic cavity is filled with a black viscous substance and histologically the tumor is composed of adamantinomatous epithelium and areas of calcification and necrosis. Papillary craniopharyngiomas occur in adults, and histologically feature a squamous epithelium with papillations. (From Joynt, Clinical Neurology, 1998, Ch14, p50) | 0 | 5.6 | 29 | 0 |
Colitis Inflammation of the COLON section of the large intestine (INTESTINE, LARGE), usually with symptoms such as DIARRHEA (often with blood and mucus), ABDOMINAL PAIN, and FEVER. | 0 | 4.45 | 8 | 0 |
Ovine Diseases [description not available] | 0 | 3.24 | 6 | 0 |
Ectopic Lymph Nodes [description not available] | 0 | 2.31 | 1 | 0 |
Experimental Neoplasms [description not available] | 0 | 7.34 | 77 | 0 |
Cancer of Testis [description not available] | 0 | 7.5 | 89 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 7.5 | 89 | 0 |
Androgen-Independent Prostatic Cancer [description not available] | 0 | 3.23 | 1 | 0 |
Prostatic Neoplasms, Castration-Resistant Tumors or cancer of the PROSTATE which can grow in the presence of low or residual amount of androgen hormones such as TESTOSTERONE. | 0 | 3.23 | 1 | 0 |
Dermoid [description not available] | 0 | 5.72 | 20 | 0 |
Peritoneal Diseases Pathological processes involving the PERITONEUM. | 0 | 3.88 | 12 | 0 |
Adrenal Cancer [description not available] | 0 | 5.27 | 20 | 0 |
Foot Diseases Anatomical and functional disorders affecting the foot. | 0 | 6.7 | 25 | 0 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 6.44 | 26 | 0 |
Gastric Ulcer [description not available] | 0 | 4.3 | 7 | 0 |
Stomach Ulcer Ulceration of the GASTRIC MUCOSA due to contact with GASTRIC JUICE. It is often associated with HELICOBACTER PYLORI infection or consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 4.3 | 7 | 0 |
Cancer of Jaw [description not available] | 0 | 7.59 | 76 | 0 |
Keratosis Seborrheica [description not available] | 0 | 5.14 | 17 | 0 |
Keratosis, Seborrheic Benign eccrine poromas that present as multiple oval, brown-to-black plaques, located mostly on the chest and back. The age of onset is usually in the fourth or fifth decade. | 0 | 5.14 | 17 | 0 |
Cystosarcoma Phyllodes [description not available] | 0 | 3.94 | 13 | 0 |
Chronic Lung Injury [description not available] | 0 | 2.31 | 1 | 0 |
Injuries, Spinal Cord [description not available] | 0 | 3.31 | 6 | 0 |
Spinal Cord Injuries Penetrating and non-penetrating injuries to the spinal cord resulting from traumatic external forces (e.g., WOUNDS, GUNSHOT; WHIPLASH INJURIES; etc.). | 0 | 3.31 | 6 | 0 |
Extravascular Hemolysis [description not available] | 0 | 3.11 | 5 | 0 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 3.11 | 5 | 0 |
Gastrointestinal Stromal Neoplasm [description not available] | 0 | 5.84 | 15 | 0 |
Gastrointestinal Stromal Tumors All tumors in the GASTROINTESTINAL TRACT arising from mesenchymal cells (MESODERM) except those of smooth muscle cells (LEIOMYOMA) or Schwann cells (SCHWANNOMA). | 0 | 5.84 | 15 | 0 |
Apoplexy [description not available] | 0 | 2.15 | 1 | 0 |
Pulmonary Arterial Remodeling [description not available] | 0 | 2.15 | 1 | 0 |
Fetal Growth Restriction [description not available] | 0 | 4.3 | 7 | 0 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 4.21 | 17 | 0 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 4.3 | 7 | 0 |
Pre-Eclampsia A complication of PREGNANCY, characterized by a complex of symptoms including maternal HYPERTENSION and PROTEINURIA with or without pathological EDEMA. Symptoms may range between mild and severe. Pre-eclampsia usually occurs after the 20th week of gestation, but may develop before this time in the presence of trophoblastic disease. | 0 | 4.21 | 17 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 2.94 | 4 | 0 |
Stroke A group of pathological conditions characterized by sudden, non-convulsive loss of neurological function due to BRAIN ISCHEMIA or INTRACRANIAL HEMORRHAGES. Stroke is classified by the type of tissue NECROSIS, such as the anatomic location, vasculature involved, etiology, age of the affected individual, and hemorrhagic vs. non-hemorrhagic nature. (From Adams et al., Principles of Neurology, 6th ed, pp777-810) | 0 | 2.15 | 1 | 0 |
Anhidrotic Ectodermal Dysplasia [description not available] | 0 | 9.6 | 52 | 0 |
Bladder Diseases [description not available] | 0 | 6.88 | 11 | 1 |
Giant Axonal Neuropathy Rare autosomal recessive disorder of INTERMEDIATE FILAMENT PROTEINS. The disease is caused by mutations in the gene that codes gigaxonin protein. The mutations result in disorganization of axonal NEUROFILAMENT PROTEINS, formation of the characteristic giant axons, and progressive neuropathy. The clinical features of the disease include early-onset progressive peripheral motor and sensory neuropathies often associated with central nervous system involvement (INTELLECTUAL DISABILITY, seizures, DYSMETRIA, and CONGENITAL NYSTAGMUS). | 0 | 2.57 | 2 | 0 |
Conjunctival Neoplasms Tumors or cancer of the CONJUNCTIVA. | 0 | 4.08 | 15 | 0 |
Cancer of Oropharnyx [description not available] | 0 | 6.01 | 16 | 0 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 6.01 | 16 | 0 |
Acne [description not available] | 0 | 10.01 | 53 | 3 |
Acne Vulgaris A chronic disorder of the pilosebaceous apparatus associated with an increase in sebum secretion. It is characterized by open comedones (blackheads), closed comedones (whiteheads), and pustular nodules. The cause is unknown, but heredity and age are predisposing factors. | 0 | 10.01 | 53 | 3 |
Condition, Preneoplastic [description not available] | 0 | 11.31 | 180 | 0 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 11.31 | 180 | 0 |
Fibroadenoma An adenoma containing fibrous tissue. It should be differentiated from ADENOFIBROMA which is a tumor composed of connective tissue (fibroma) containing glandular (adeno-) structures. (From Dorland, 27th ed) | 0 | 5.12 | 17 | 0 |
Atresia, Biliary [description not available] | 0 | 5.68 | 19 | 1 |
Biliary Atresia Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually, biliary atresia is found in infants and accounts for one third of the neonatal cholestatic JAUNDICE. | 0 | 5.68 | 19 | 1 |
Carcinoma, Colloid [description not available] | 0 | 9.25 | 76 | 0 |
Adenocarcinoma, Papillary An adenocarcinoma containing finger-like processes of vascular connective tissue covered by neoplastic epithelium, projecting into cysts or the cavity of glands or follicles. It occurs most frequently in the ovary and thyroid gland. (Stedman, 25th ed) | 0 | 4.61 | 26 | 0 |
Adenocarcinoma, Mucinous An adenocarcinoma producing mucin in significant amounts. (From Dorland, 27th ed) | 0 | 9.25 | 76 | 0 |
Disease Exacerbation [description not available] | 0 | 15.77 | 159 | 15 |
Atypical Lipomatous Tumor [description not available] | 0 | 4.79 | 12 | 0 |
Liposarcoma A malignant tumor derived from primitive or embryonal lipoblastic cells. It may be composed of well-differentiated fat cells or may be dedifferentiated: myxoid (LIPOSARCOMA, MYXOID), round-celled, or pleomorphic, usually in association with a rich network of capillaries. Recurrences are common and dedifferentiated liposarcomas metastasize to the lungs or serosal surfaces. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 4.79 | 12 | 0 |
Cancer of Granulosa Cells [description not available] | 0 | 5.1 | 17 | 0 |
Gynandroblastoma A sex cord-gonadal stromal tumor, composed of cells of both the OVARY and the TESTIS. It produces both male and female GONADAL STEROID HORMONES. | 0 | 6.48 | 24 | 0 |
Androblastoma [description not available] | 0 | 3.72 | 10 | 0 |
Theca Cell Tumor [description not available] | 0 | 4.02 | 5 | 0 |
Sex Cord-Gonadal Stromal Tumors Neoplasms derived from the primitive sex cord or gonadal stromal cells of the embryonic GONADS. They are classified by their presumed histogenesis and differentiation. From the sex cord, there are SERTOLI CELL TUMOR and GRANULOSA CELL TUMOR; from the gonadal stroma, LEYDIG CELL TUMOR and THECOMA. These tumors may be identified in either the OVARY or the TESTIS. | 0 | 6.48 | 24 | 0 |
Adenosis of Breast [description not available] | 0 | 5.25 | 20 | 0 |
Fibrocystic Breast Disease A common and benign breast disease characterized by varying degree of fibrocystic changes in the breast tissue. There are three major patterns of morphological changes, including FIBROSIS, formation of CYSTS, and proliferation of glandular tissue (adenosis). The fibrocystic breast has a dense irregular, lumpy, bumpy consistency. | 0 | 5.25 | 20 | 0 |
Hamartoma A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area. | 0 | 7.48 | 47 | 0 |
Hand Dermatosis [description not available] | 0 | 4.38 | 21 | 0 |
Hand Dermatoses Skin diseases involving the HANDS. | 0 | 4.38 | 21 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 13.29 | 121 | 3 |
Arthritis, Rheumatoid A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated. | 0 | 13.29 | 121 | 3 |
Chromosomal Translocation [description not available] | 0 | 6.77 | 26 | 0 |
Lymphoma, Primary Effusion A rare neoplasm of large B-cells usually presenting as serious effusions without detectable tumor masses. The most common sites of involvement are the pleural, pericardial, and peritoneal cavities. It is associated with HUMAN HERPESVIRUS 8, most often occurring in the setting of immunodeficiency. | 0 | 2.55 | 2 | 0 |
Periapical Cyst [description not available] | 0 | 6.32 | 37 | 0 |
Jaw Cysts Saccular lesions lined with epithelium and contained within pathologically formed cavities in the jaw; also nonepithelial cysts (pseudocysts) as they apply to the jaw, e.g., traumatic or solitary cyst, static bone cavity, and aneurysmal bone cyst. True jaw cysts are classified as odontogenic or nonodontogenic. | 0 | 5.32 | 13 | 0 |
Dentigerous Cyst Most common follicular odontogenic cyst. Occurs in relation to a partially erupted or unerupted tooth with at least the crown of the tooth to which the cyst is attached protruding into the cystic cavity. May give rise to an ameloblastoma and, in rare instances, undergo malignant transformation. | 0 | 5.85 | 38 | 0 |
Alopecia Cicatrisata [description not available] | 0 | 10.13 | 60 | 2 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 10.13 | 60 | 2 |
Amnionitis [description not available] | 0 | 2.46 | 2 | 0 |
Chorioamnionitis INFLAMMATION of the placental membranes (CHORION; AMNION) and connected tissues such as fetal BLOOD VESSELS and UMBILICAL CORD. It is often associated with intrauterine ascending infections during PREGNANCY. | 0 | 2.46 | 2 | 0 |
Neoplasms, Pleural [description not available] | 0 | 9.59 | 110 | 0 |
Cardiac Tamponade Compression of the heart by accumulated fluid (PERICARDIAL EFFUSION) or blood (HEMOPERICARDIUM) in the PERICARDIUM surrounding the heart. The affected cardiac functions and CARDIAC OUTPUT can range from minimal to total hemodynamic collapse. | 0 | 2.74 | 3 | 0 |
Barrett Epithelium [description not available] | 0 | 7.52 | 48 | 0 |
Esophageal Reflux [description not available] | 0 | 3.82 | 11 | 0 |
Barrett Esophagus A condition with damage to the lining of the lower ESOPHAGUS resulting from chronic acid reflux (ESOPHAGITIS, REFLUX). Through the process of metaplasia, the squamous cells are replaced by a columnar epithelium with cells resembling those of the INTESTINE or the salmon-pink mucosa of the STOMACH. Barrett's columnar epithelium is a marker for severe reflux and precursor to ADENOCARCINOMA of the esophagus. | 0 | 7.52 | 48 | 0 |
Gastroesophageal Reflux Retrograde flow of gastric juice (GASTRIC ACID) and/or duodenal contents (BILE ACIDS; PANCREATIC JUICE) into the distal ESOPHAGUS, commonly due to incompetence of the LOWER ESOPHAGEAL SPHINCTER. | 0 | 3.82 | 11 | 0 |
Short Bowel Syndrome A malabsorption syndrome resulting from extensive operative resection of the SMALL INTESTINE, the absorptive region of the GASTROINTESTINAL TRACT. | 0 | 2.48 | 2 | 0 |
Chronic Kidney Failure [description not available] | 0 | 5.01 | 15 | 0 |
Kidney Failure, Chronic The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION. | 0 | 5.01 | 15 | 0 |
Glenoid Labral Tears [description not available] | 0 | 2.17 | 1 | 0 |
Rotator Cuff Injuries Injuries to the ROTATOR CUFF of the shoulder joint. | 0 | 2.17 | 1 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 3.26 | 6 | 0 |
Osteoporosis Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis. | 0 | 3.26 | 6 | 0 |
Jaw Diseases Diseases involving the JAW. | 0 | 6.59 | 36 | 0 |
Adnexal and Skin Appendage Neoplasms [description not available] | 0 | 3.28 | 6 | 0 |
Anemia, Cooley's [description not available] | 0 | 2.17 | 1 | 0 |
beta-Thalassemia A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. | 0 | 2.17 | 1 | 0 |
Adenovirus Infections [description not available] | 0 | 2.17 | 1 | 0 |
Adenoviridae Infections Virus diseases caused by the ADENOVIRIDAE. | 0 | 2.17 | 1 | 0 |
Epiretinal Membrane A membrane on the vitreal surface of the retina resulting from the proliferation of one or more of three retinal elements: (1) fibrous astrocytes; (2) fibrocytes; and (3) RETINAL PIGMENT EPITHELIUM. Localized epiretinal membranes may occur at the posterior pole of the eye without clinical signs or may cause marked loss of vision as a result of covering, distorting, or detaching the FOVEA CENTRALIS. Epiretinal membranes may cause vascular leakage and secondary retinal edema. In younger individuals some membranes appear to be developmental in origin and occur in otherwise normal eyes. The majority occur in association with RETINAL HOLES, ocular concussions, retinal inflammation, or after ocular surgery. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p291) | 0 | 5.13 | 10 | 1 |
Diabetic Retinopathy Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION. | 0 | 4.91 | 8 | 1 |
Mixed Tumor, Malignant A malignant tumor composed of more than one type of neoplastic tissue. (Dorland, 27th ed) | 0 | 3.72 | 10 | 0 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 3.5 | 8 | 0 |
Asthma, Bronchial [description not available] | 0 | 5.67 | 10 | 2 |
Asthma A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL). | 0 | 5.67 | 10 | 2 |
Central Nervous System Neoplasm [description not available] | 0 | 5.45 | 8 | 0 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 5.45 | 8 | 0 |
Rhabdoid Tumor A rare but highly lethal childhood tumor found almost exclusively in infants. Histopathologically, it resembles RHABDOMYOSARCOMA but the tumor cells are not of myogenic origin. Although it arises primarily in the kidney, it may be found in other parts of the body. The rhabdoid cytomorphology is believed to be the expression of a very primitive malignant cell. (From Holland et al., Cancer Medicine, 3d ed, p2210) | 0 | 7.48 | 46 | 0 |
Adenocarcinoma, Sebaceous A malignant tumor composed of cells showing differentiation toward sebaceous epithelium. The tumor is solitary, firm, somewhat raised, more or less translucent, and covered with normal or slightly verrucose epidermis. It may be yellow or orange. The face and scalp are the commonest sites. The growth can be slow or rapid but metastasis is uncommon. Surgery cures most of the cases. (From Rook et al., Textbook of Dermatology, 4th ed, pp2403-4) | 0 | 4.02 | 14 | 0 |
Neoplasms, Sebaceous Gland [description not available] | 0 | 6.62 | 28 | 0 |
Bile Duct Obstruction [description not available] | 0 | 5.95 | 25 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 5.95 | 25 | 0 |
Mouth, Edentulous Total lack of teeth through disease or extraction. | 0 | 4.59 | 10 | 0 |
Cancer of the Tongue [description not available] | 0 | 9.46 | 86 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 9.46 | 86 | 0 |
Caries, Dental [description not available] | 0 | 4.09 | 3 | 1 |
Tooth Erosion Progressive loss of the hard substance of a tooth by chemical processes that do not involve bacterial action. (Jablonski, Dictionary of Dentistry, 1992, p296) | 0 | 2.41 | 2 | 0 |
Dental Caries Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp. | 0 | 4.09 | 3 | 1 |
Adnexal Diseases Diseases of the uterine appendages (ADNEXA UTERI) including diseases involving the OVARY, the FALLOPIAN TUBES, and ligaments of the uterus (BROAD LIGAMENT; ROUND LIGAMENT). | 0 | 4.33 | 7 | 0 |
Cancer of Digestive System [description not available] | 0 | 6.16 | 12 | 0 |
Digestive System Neoplasms Tumors or cancer of the DIGESTIVE SYSTEM. | 0 | 6.16 | 12 | 0 |
Minimal Disease, Residual [description not available] | 0 | 7.73 | 37 | 1 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 5.59 | 17 | 0 |
Endometrial Stromal Sarcoma [description not available] | 0 | 3.3 | 6 | 0 |
Sarcoma, Endometrial Stromal A highly malignant subset of neoplasms arising from the endometrial stroma. Tumors in this group infiltrate the stroma with a wide range of atypia cells and numerous mitoses. They are capable of widespread metastases (NEOPLASM METASTASIS). | 0 | 3.3 | 6 | 0 |
Polyps Discrete abnormal tissue masses that protrude into the lumen of the DIGESTIVE TRACT or the RESPIRATORY TRACT. Polyps can be spheroidal, hemispheroidal, or irregular mound-shaped structures attached to the MUCOUS MEMBRANE of the lumen wall either by a stalk, pedunculus, or by a broad base. | 0 | 5.95 | 18 | 0 |
Gastric Diseases [description not available] | 0 | 5.2 | 11 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 2.82 | 3 | 0 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 2.82 | 3 | 0 |
Stasis Ulcer [description not available] | 0 | 5.6 | 6 | 1 |
Varicose Ulcer Skin breakdown or ulceration in the drainage area of a VARICOSE VEIN, usually in the leg. | 0 | 5.6 | 6 | 1 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 5.65 | 13 | 0 |
Rhabdomyosarcoma A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) | 0 | 9.22 | 47 | 1 |
Dry Eye [description not available] | 0 | 4.48 | 8 | 0 |
Dry Eye Syndromes Corneal and conjunctival dryness due to deficient tear production, predominantly in menopausal and post-menopausal women. Filamentary keratitis or erosion of the conjunctival and corneal epithelium may be caused by these disorders. Sensation of the presence of a foreign body in the eye and burning of the eyes may occur. | 0 | 4.48 | 8 | 0 |
Aneuploid [description not available] | 0 | 8.71 | 42 | 2 |
Anasarca [description not available] | 0 | 5.13 | 18 | 0 |
Allergic Reaction [description not available] | 0 | 5.41 | 5 | 1 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 5.13 | 18 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 5.41 | 5 | 1 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 4.14 | 6 | 0 |
Kidney Failure A severe irreversible decline in the ability of kidneys to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. | 0 | 3.11 | 5 | 0 |
Renal Insufficiency Conditions in which the KIDNEYS perform below the normal level in the ability to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. Renal insufficiency can be classified by the degree of kidney damage (as measured by the level of PROTEINURIA) and reduction in GLOMERULAR FILTRATION RATE. | 0 | 3.11 | 5 | 0 |
Acanthosis Nigricans A circumscribed melanosis consisting of a brown-pigmented, velvety verrucosity or fine papillomatosis appearing in the axillae and other body folds. It occurs in association with endocrine disorders, underlying malignancy, administration of certain drugs, or as in inherited disorder. | 0 | 2.7 | 3 | 0 |
Atrophy of Gingiva [description not available] | 0 | 23.68 | 300 | 183 |
Acute Post-operative Pain [description not available] | 0 | 12.26 | 29 | 17 |
Pain, Postoperative Pain during the period after surgery. | 0 | 12.26 | 29 | 17 |
Connective and Soft Tissue Neoplasms [description not available] | 0 | 2.17 | 1 | 0 |
B16 Melanoma [description not available] | 0 | 2.92 | 4 | 0 |
Fuch's Endothelial Dystrophy [description not available] | 0 | 2.77 | 3 | 0 |
Fuchs' Endothelial Dystrophy Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain. | 0 | 2.77 | 3 | 0 |
Verruca [description not available] | 0 | 7 | 35 | 0 |
Scalp Dermatoses Skin diseases involving the SCALP. | 0 | 5.98 | 19 | 0 |
Warts Benign epidermal proliferations or tumors; some are viral in origin. | 0 | 7 | 35 | 0 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 2.93 | 4 | 0 |
Recrudescence [description not available] | 0 | 12.9 | 111 | 3 |
Lacrimal Duct Obstruction Interference with the secretion of tears by the lacrimal glands. Obstruction of the LACRIMAL SAC or NASOLACRIMAL DUCT causing acute or chronic inflammation of the lacrimal sac (DACRYOCYSTITIS). It is caused also in infants by failure of the nasolacrimal duct to open into the inferior meatus and occurs about the third week of life. In adults occlusion may occur spontaneously or after injury or nasal disease. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p250) | 0 | 2.61 | 2 | 0 |
Keratoacanthoma A benign, non-neoplastic, usually self-limiting epithelial lesion closely resembling squamous cell carcinoma clinically and histopathologically. It occurs in solitary, multiple, and eruptive forms. The solitary and multiple forms occur on sunlight exposed areas and are identical histologically; they affect primarily white males. The eruptive form usually involves both sexes and appears as a generalized papular eruption. | 0 | 7.17 | 35 | 0 |
Implant Capsular Contracture The shrinkage of the foreign body encapsulation scar tissue that forms around artificial implants imbedded in body tissues. | 0 | 2.17 | 1 | 0 |
Epiphora [description not available] | 0 | 5.1 | 17 | 0 |
Lacrimal Apparatus Diseases Diseases of the LACRIMAL APPARATUS. | 0 | 5.1 | 17 | 0 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 6.3 | 19 | 0 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 10.24 | 35 | 1 |
Diabetes Mellitus, Type 2 A subclass of DIABETES MELLITUS that is not INSULIN-responsive or dependent (NIDDM). It is characterized initially by INSULIN RESISTANCE and HYPERINSULINEMIA; and eventually by GLUCOSE INTOLERANCE; HYPERGLYCEMIA; and overt diabetes. Type II diabetes mellitus is no longer considered a disease exclusively found in adults. Patients seldom develop KETOSIS but often exhibit OBESITY. | 0 | 6.3 | 19 | 0 |
Wounds and Injuries Damage inflicted on the body as the direct or indirect result of an external force, with or without disruption of structural continuity. | 0 | 10.24 | 35 | 1 |
Eyelid Neoplasms Tumors of cancer of the EYELIDS. | 0 | 6.57 | 27 | 0 |
Hemangioma, Capillary A dull red, firm, dome-shaped hemangioma, sharply demarcated from surrounding skin, usually located on the head and neck, which grows rapidly and generally undergoes regression and involution without scarring. It is caused by proliferation of immature capillary vessels in active stroma, and is usually present at birth or occurs within the first two or three months of life. (Dorland, 27th ed) | 0 | 2.44 | 2 | 0 |
Coin Lesion, Pulmonary [description not available] | 0 | 3.86 | 4 | 0 |
Chronic Hepatitis B [description not available] | 0 | 3.42 | 7 | 0 |
Hepatitis B, Chronic INFLAMMATION of the LIVER in humans caused by HEPATITIS B VIRUS lasting six months or more. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 3.42 | 7 | 0 |
Cancer of Penis [description not available] | 0 | 4.12 | 16 | 0 |
Penile Neoplasms Cancers or tumors of the PENIS or of its component tissues. | 0 | 4.12 | 16 | 0 |
Pyoderma Gangrenosum An idiopathic, rapidly evolving, and severely debilitating disease occurring most commonly in association with chronic ulcerative colitis. It is characterized by the presence of boggy, purplish ulcers with undermined borders, appearing mostly on the legs. The majority of cases are in people between 40 and 60 years old. Its etiology is unknown. | 0 | 2.47 | 2 | 0 |
Leg Ulcer Ulceration of the skin and underlying structures of the lower extremity. About 90% of the cases are due to venous insufficiency (VARICOSE ULCER), 5% to arterial disease, and the remaining 5% to other causes. | 0 | 7.18 | 12 | 1 |
Asialia [description not available] | 0 | 4.32 | 4 | 1 |
Xerostomia Decreased salivary flow. | 0 | 4.32 | 4 | 1 |
Osteogenic Sarcoma [description not available] | 0 | 4.44 | 22 | 0 |
Osteosarcoma A sarcoma originating in bone-forming cells, affecting the ends of long bones. It is the most common and most malignant of sarcomas of the bones, and occurs chiefly among 10- to 25-year-old youths. (From Stedman, 25th ed) | 0 | 4.44 | 22 | 0 |
Fibroepithelial Neoplasms [description not available] | 0 | 3.66 | 3 | 0 |
Basal Cell Cancer [description not available] | 0 | 8.75 | 43 | 0 |
Maxillary Neoplasms Cancer or tumors of the MAXILLA or upper jaw. | 0 | 7.77 | 56 | 0 |
Contagious Pustular Dermatitis [description not available] | 0 | 2.42 | 2 | 0 |
Angiogranuloma [description not available] | 0 | 2.44 | 2 | 0 |
Bone Loss, Perimenopausal [description not available] | 0 | 2.21 | 1 | 0 |
Osteoporosis, Postmenopausal Metabolic disorder associated with fractures of the femoral neck, vertebrae, and distal forearm. It occurs commonly in women within 15-20 years after menopause, and is caused by factors associated with menopause including estrogen deficiency. | 0 | 2.21 | 1 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 7.07 | 37 | 0 |
Leiomyosarcoma A sarcoma containing large spindle cells of smooth muscle. Although it rarely occurs in soft tissue, it is common in the viscera. It is the most common soft tissue sarcoma of the gastrointestinal tract and uterus. The median age of patients is 60 years. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1865) | 0 | 7.07 | 37 | 0 |
Encapsulating Peritoneal Sclerosis [description not available] | 0 | 3.95 | 4 | 0 |
Allergy, Food [description not available] | 0 | 3.37 | 2 | 0 |
Food Hypersensitivity Gastrointestinal disturbances, skin eruptions, or shock due to allergic reactions to allergens in food. | 0 | 3.37 | 2 | 0 |
Polyomavirus Infections Infections with POLYOMAVIRUS, which are often cultured from the urine of kidney transplant patients. Excretion of BK VIRUS is associated with ureteral strictures and CYSTITIS, and that of JC VIRUS with progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL). | 0 | 4.41 | 4 | 0 |
Abnormalities, Congenital [description not available] | 0 | 3.24 | 6 | 0 |
Complication, Postoperative [description not available] | 0 | 11.17 | 35 | 8 |
Lichen Nitidus A chronic inflammatory disease characterized by shiny, flat-topped, usually flesh-colored micropapules no larger than the head of a pin. Lesions are localized in the early stages, found chiefly on the lower abdomen, penis, and inner surface of the thighs. Distribution may become generalized as the disease progresses. | 0 | 2.21 | 1 | 0 |
Fibroma, Shope [description not available] | 0 | 5.86 | 38 | 0 |
Postoperative Complications Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery. | 0 | 11.17 | 35 | 8 |
Atypical Endometrial Hyperplasia A benign form of endometrial hyperplasia with increased number of cells with atypia. The atypical cells are large and irregular and have an increased nuclear/cytoplasmic ratio. The risk of progression to endometrial carcinoma rises with the increasing degree of cell atypia. | 0 | 4.04 | 5 | 0 |
Endometrial Hyperplasia Benign proliferation of the ENDOMETRIUM in the UTERUS. Endometrial hyperplasia is classified by its cytology and glandular tissue. There are simple, complex (adenomatous without atypia), and atypical hyperplasia representing also the ascending risk of becoming malignant. | 0 | 4.04 | 5 | 0 |
Neoplasms, Sweat Gland [description not available] | 0 | 8.75 | 117 | 0 |
Acantholysis Bullosa [description not available] | 0 | 8.74 | 52 | 0 |
Epidermolysis Bullosa Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. | 0 | 8.74 | 52 | 0 |
Biliary Tract Cancer [description not available] | 0 | 7.04 | 16 | 0 |
Biliary Tract Neoplasms Tumors or cancer in the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 7.04 | 16 | 0 |
Angiogenesis, Pathologic [description not available] | 0 | 8.98 | 52 | 1 |
Acute Brain Injuries [description not available] | 0 | 2.76 | 3 | 0 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 2.21 | 1 | 0 |
Brain Injuries Acute and chronic (see also BRAIN INJURIES, CHRONIC) injuries to the brain, including the cerebral hemispheres, CEREBELLUM, and BRAIN STEM. Clinical manifestations depend on the nature of injury. Diffuse trauma to the brain is frequently associated with DIFFUSE AXONAL INJURY or COMA, POST-TRAUMATIC. Localized injuries may be associated with NEUROBEHAVIORAL MANIFESTATIONS; HEMIPARESIS, or other focal neurologic deficits. | 0 | 2.76 | 3 | 0 |
Cerebral Hemorrhage Bleeding into one or both CEREBRAL HEMISPHERES including the BASAL GANGLIA and the CEREBRAL CORTEX. It is often associated with HYPERTENSION and CRANIOCEREBRAL TRAUMA. | 0 | 2.21 | 1 | 0 |
Chronic Hepatitis C [description not available] | 0 | 3.97 | 13 | 0 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 3.97 | 13 | 0 |
Gingival Overgrowth Excessive growth of the gingiva either by an increase in the size of the constituent cells (GINGIVAL HYPERTROPHY) or by an increase in their number (GINGIVAL HYPERPLASIA). (From Jablonski's Dictionary of Dentistry, 1992, p574) | 0 | 2.45 | 2 | 0 |
Inguinal Hernia [description not available] | 0 | 2.73 | 3 | 0 |
Hernia, Inguinal An abdominal hernia with an external bulge in the GROIN region. It can be classified by the location of herniation. Indirect inguinal hernias occur through the internal inguinal ring. Direct inguinal hernias occur through defects in the ABDOMINAL WALL (transversalis fascia) in Hesselbach's triangle. The former type is commonly seen in children and young adults; the latter in adults. | 0 | 2.73 | 3 | 0 |
Vesicoureteral Reflux [description not available] | 0 | 2.48 | 2 | 0 |
Abnormalities, Urogenital [description not available] | 0 | 2.47 | 2 | 0 |
Vesico-Ureteral Reflux Retrograde flow of urine from the URINARY BLADDER into the URETER. This is often due to incompetence of the vesicoureteral valve leading to ascending bacterial infection into the KIDNEY. | 0 | 2.48 | 2 | 0 |
Wounds, Penetrating Wounds caused by objects penetrating the skin. | 0 | 4.04 | 5 | 0 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 9.89 | 33 | 5 |
Symptom Cluster [description not available] | 0 | 10.05 | 77 | 1 |
Syndrome A characteristic symptom complex. | 0 | 10.05 | 77 | 1 |
Acquired Meningocele [description not available] | 0 | 2.92 | 4 | 0 |
Attachment Loss, Periodontal [description not available] | 0 | 22.37 | 193 | 121 |
Pocket, Periodontal [description not available] | 0 | 18.88 | 161 | 121 |
Periodontal Pocket An abnormal extension of a gingival sulcus accompanied by the apical migration of the epithelial attachment and bone resorption. | 0 | 18.88 | 161 | 121 |
Hemorrhage, Gingival [description not available] | 0 | 11.87 | 20 | 12 |
Jaw, Edentulous The total absence of teeth from either the mandible or the maxilla, but not both. Total absence of teeth from both is MOUTH, EDENTULOUS. Partial absence of teeth in either is JAW, EDENTULOUS, PARTIALLY. | 0 | 7.87 | 9 | 2 |
Dehiscence, Surgical Wound [description not available] | 0 | 4.12 | 3 | 1 |
Gingival Hemorrhage The flowing of blood from the marginal gingival area, particularly the sulcus, seen in such conditions as GINGIVITIS, marginal PERIODONTITIS, injury, and ASCORBIC ACID DEFICIENCY. | 0 | 11.87 | 20 | 12 |
Deaf Mutism [description not available] | 0 | 3.61 | 3 | 0 |
Disseminated Superficial Actinic Porokeratosis [description not available] | 0 | 4.53 | 5 | 0 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 3.61 | 3 | 0 |
Keratitis Inflammation of the cornea. | 0 | 6.05 | 11 | 1 |
Porokeratosis A heritable disorder of faulty keratinization characterized by the proliferation of abnormal clones of KERATINOCYTES and lesions showing varying atrophic patches surrounded by an elevated, keratotic border. These keratotic lesions can progress to overt cutaneous neoplasm. Several clinical variants are recognized, including porokeratosis of Mibelli, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis, and punctate porokeratosis. | 0 | 4.53 | 5 | 0 |
Intraepithelial Prostatic Neoplasia [description not available] | 0 | 7.7 | 36 | 1 |
Prostatic Intraepithelial Neoplasia A premalignant change arising in the prostatic epithelium, regarded as the most important and most likely precursor of prostatic adenocarcinoma. The neoplasia takes the form of an intra-acinar or ductal proliferation of secretory cells with unequivocal nuclear anaplasia, which corresponds to nuclear grade 2 and 3 invasive prostate cancer. | 0 | 7.7 | 36 | 1 |
Carcinoma, Oat Cell [description not available] | 0 | 11.1 | 170 | 1 |
Carcinoma, Small Cell An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7) | 0 | 11.1 | 170 | 1 |
Fifth Phacomatosis [description not available] | 0 | 6.62 | 28 | 0 |
Basal Cell Nevus Syndrome Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant. | 0 | 6.62 | 28 | 0 |
Mycosis Fungoides A chronic, malignant T-cell lymphoma of the skin. In the late stages, the LYMPH NODES and viscera are affected. | 0 | 4.45 | 5 | 0 |
Adipocere [description not available] | 0 | 2.9 | 4 | 0 |
Age-Related Macular Degeneration [description not available] | 0 | 5.2 | 11 | 0 |
Drusen, Retinal [description not available] | 0 | 2.08 | 1 | 0 |
Macular Degeneration Degenerative changes in the RETINA usually of older adults which results in a loss of vision in the center of the visual field (the MACULA LUTEA) because of damage to the retina. It occurs in dry and wet forms. | 0 | 5.2 | 11 | 0 |
Gait Disorders, Animal [description not available] | 0 | 4.32 | 7 | 0 |
Cancer of Lip [description not available] | 0 | 6.62 | 28 | 0 |
Acantholytic Dyskeratotic Epidermal Nevi [description not available] | 0 | 10.97 | 39 | 3 |
Teeth, Impacted [description not available] | 0 | 4.56 | 9 | 0 |
Molar, Fourth [description not available] | 0 | 2.08 | 1 | 0 |
Plasma Cell Tumor [description not available] | 0 | 3.77 | 11 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 3.77 | 11 | 0 |
Abortion, Missed The retention in the UTERUS of a dead FETUS two months or more after its DEATH. | 0 | 2.73 | 3 | 0 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 5.59 | 17 | 0 |
Chemical and Drug Induced Liver Injury, Chronic Liver disease lasting six months or more, caused by an adverse effect of a drug or chemical. The adverse effect may be caused by drugs, drug metabolites, chemicals from the environment, or an idiosyncratic response. | 0 | 2.08 | 1 | 0 |
Acute Disease Disease having a short and relatively severe course. | 0 | 5.3 | 21 | 0 |
Chemical and Drug Induced Liver Injury A spectrum of clinical liver diseases ranging from mild biochemical abnormalities to ACUTE LIVER FAILURE, caused by drugs, drug metabolites, herbal and dietary supplements and chemicals from the environment. | 0 | 5.59 | 17 | 0 |
Mixed Pineocytoma-Pineoblastoma [description not available] | 0 | 3 | 4 | 0 |
Anaplastic Ependymoma [description not available] | 0 | 6.13 | 22 | 0 |
Ependymoma Glioma derived from EPENDYMOGLIAL CELLS that tend to present as malignant intracranial tumors in children and as benign intraspinal neoplasms in adults. It may arise from any level of the ventricular system or central canal of the spinal cord. Intracranial ependymomas most frequently originate in the FOURTH VENTRICLE and histologically are densely cellular tumors which may contain ependymal tubules and perivascular pseudorosettes. Spinal ependymomas are usually benign papillary or myxopapillary tumors. (From DeVita et al., Principles and Practice of Oncology, 5th ed, p2018; Escourolle et al., Manual of Basic Neuropathology, 2nd ed, pp28-9) | 0 | 6.13 | 22 | 0 |
Pinealoma Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670) | 0 | 3 | 4 | 0 |
Cancer of the Urinary Tract [description not available] | 0 | 6.1 | 21 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 5.21 | 19 | 0 |
Anesthesia A state characterized by loss of feeling or sensation. This depression of nerve function is usually the result of pharmacologic action and is induced to allow performance of surgery or other painful procedures. | 0 | 2.08 | 1 | 0 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 5.06 | 43 | 0 |
Miliaria A syndrome of cutaneous changes associated with sweat retention and extravasation of sweat at different levels in the skin. Miliaria rubra, or prickly heat, results from apocrine duct obstruction. The sweat then seeps into the epidermis, producing pruritic erythematous papulovesicles. (From Dorland, 27th ed) | 0 | 2.65 | 3 | 0 |
Epithelial Ovarian Cancer [description not available] | 0 | 3.68 | 3 | 0 |
Carcinoma, Ovarian Epithelial A malignant neoplasm that originates in cells on the surface EPITHELIUM of the ovary and is the most common form of ovarian cancer. There are five histologic subtypes: papillary serous, endometrioid, mucinous, clear cell, and transitional cell. Mutations in BRCA1, OPCML, PRKN, PIK3CA, AKT1, CTNNB1, RRAS2, and CDH1 genes are associated with this cancer. | 0 | 3.68 | 3 | 0 |
Argentaffinoma [description not available] | 0 | 8.08 | 67 | 0 |
Carcinoid Tumor A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182) | 0 | 8.08 | 67 | 0 |
Chronic Illness [description not available] | 0 | 9.97 | 83 | 1 |
Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). | 0 | 9.97 | 83 | 1 |
Musculoskeletal Pain Discomfort stemming from muscles, LIGAMENTS, tendons, and bones. | 0 | 3.47 | 1 | 1 |
Angiomyolipoma A benign tumor containing vascular, adipose, and muscle elements. It occurs most often in the kidney with smooth muscle elements (angiolipoleiomyoma) in association with tuberous sclerosis. (Dorland, 27th ed) | 0 | 5.02 | 9 | 0 |
Angiomyxoma [description not available] | 0 | 5.77 | 15 | 0 |
Cancer, Embryonal [description not available] | 0 | 6.91 | 50 | 0 |
Cancer of the Vagina [description not available] | 0 | 7.02 | 21 | 0 |
Neoplasms, Germ Cell and Embryonal Neoplasms composed of primordial GERM CELLS of embryonic GONADS or of elements of the germ layers of the EMBRYO, MAMMALIAN. The concept does not refer to neoplasms located in the gonads or present in an embryo or FETUS. | 0 | 6.91 | 50 | 0 |
Vaginal Neoplasms Tumors or cancer of the VAGINA. | 0 | 7.02 | 21 | 0 |
Cholangiocellular Carcinoma [description not available] | 0 | 7.8 | 64 | 0 |
Cholangiocarcinoma A malignant tumor arising from the epithelium of the BILE DUCTS. | 0 | 7.8 | 64 | 0 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 5.57 | 17 | 0 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 5.57 | 17 | 0 |
Intertrigo A superficial dermatitis occurring on skin surfaces in contact with each other, such as the axillae, neck creases, intergluteal fold, between the toes, etc. Obesity is a predisposing factor. The condition is caused by moisture and friction and is characterized by erythema, maceration, burning, and exudation. | 0 | 2.08 | 1 | 0 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 3.12 | 5 | 0 |
Weight Reduction [description not available] | 0 | 2.93 | 4 | 0 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 2.93 | 4 | 0 |
Fibroid [description not available] | 0 | 4.24 | 18 | 0 |
Adenomyoma A benign neoplasm of muscle (usually smooth muscle) with glandular elements. It occurs most frequently in the uterus and uterine ligaments. (Stedman, 25th ed) | 0 | 2.94 | 4 | 0 |
Adenomatoid Tumor A small, circumscribed, benign tumor of the genital tract, composed of small glandlike spaces lined by flattened or cuboidal mesothelium-like cells. (From Dorland, 27th ed) | 0 | 5.32 | 21 | 0 |
Lymphatic Vessel Tumors Neoplasms composed of lymphoid tissue, a lattice work of reticular tissue the interspaces of which contain lymphocytes. The concept does not refer to neoplasms located in lymphatic vessels. | 0 | 2.08 | 1 | 0 |
Leiomyoma A benign tumor derived from smooth muscle tissue, also known as a fibroid tumor. They rarely occur outside of the UTERUS and the GASTROINTESTINAL TRACT but can occur in the SKIN and SUBCUTANEOUS TISSUE, probably arising from the smooth muscle of small blood vessels in these tissues. | 0 | 4.24 | 18 | 0 |
Cervix Dysplasia [description not available] | 0 | 5.8 | 35 | 0 |
Uterine Cervical Dysplasia Abnormal development of immature squamous EPITHELIAL CELLS of the UTERINE CERVIX, a term used to describe premalignant cytological changes in the cervical EPITHELIUM. These atypical cells do not penetrate the epithelial BASEMENT MEMBRANE. | 0 | 5.8 | 35 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 6.37 | 39 | 0 |
Synovioma [description not available] | 0 | 8.05 | 73 | 0 |
Sarcoma, Synovial A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363) | 0 | 8.05 | 73 | 0 |
Epulides [description not available] | 0 | 10.52 | 33 | 3 |
Gingival Diseases Diseases involving the GINGIVA. | 0 | 10.52 | 33 | 3 |
Keloid A sharply elevated, irregularly shaped, progressively enlarging scar resulting from formation of excessive amounts of collagen in the dermis during connective tissue repair. It is differentiated from a hypertrophic scar (CICATRIX, HYPERTROPHIC) in that the former does not spread to surrounding tissues. | 0 | 4.89 | 8 | 1 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 5.65 | 2 | 1 |
Leprosy, Cutaneous [description not available] | 0 | 2.08 | 1 | 0 |
Cerebral Primitive Neuroectodermal Tumor [description not available] | 0 | 4.03 | 14 | 0 |
Neuroectodermal Tumors, Primitive A group of malignant tumors of the nervous system that feature primitive cells with elements of neuronal and/or glial differentiation. Use of this term is limited by some authors to central nervous system tumors and others include neoplasms of similar origin which arise extracranially (i.e., NEUROECTODERMAL TUMORS, PRIMITIVE, PERIPHERAL). This term is also occasionally used as a synonym for MEDULLOBLASTOMA. In general, these tumors arise in the first decade of life and tend to be highly malignant. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2059) | 0 | 4.03 | 14 | 0 |
Sicca Syndrome [description not available] | 0 | 5.73 | 20 | 0 |
Sjogren's Syndrome Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis. | 0 | 5.73 | 20 | 0 |
Dental Granuloma [description not available] | 0 | 3.25 | 6 | 0 |
Leiomyomatosis The state of having multiple leiomyomas throughout the body. (Stedman, 25th ed) | 0 | 3.65 | 3 | 0 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 4.7 | 11 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 4.04 | 5 | 0 |
Cholera Infantum [description not available] | 0 | 3.41 | 7 | 0 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 3.82 | 4 | 0 |
Histiocytosis, Langerhans-Cell A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder. | 0 | 3.82 | 4 | 0 |
Colitis, Granulomatous [description not available] | 0 | 3.38 | 7 | 0 |
Cancer of ILEUM [description not available] | 0 | 4.99 | 9 | 0 |
Cancer of Jejunum [description not available] | 0 | 5.03 | 9 | 0 |
Crohn Disease A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients. | 0 | 3.38 | 7 | 0 |
Germinoma A malignant neoplasm of the germinal tissue of the GONADS; MEDIASTINUM; or pineal region. Germinomas are uniform in appearance, consisting of large, round cells with vesicular nuclei and clear or finely granular eosinophilic-staining cytoplasm. (Stedman, 265th ed; from DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1642-3) | 0 | 5.97 | 14 | 0 |
Diabetic Feet [description not available] | 0 | 4.59 | 3 | 0 |
Diabetic Foot Common foot problems in persons with DIABETES MELLITUS, caused by any combination of factors such as DIABETIC NEUROPATHIES; PERIPHERAL VASCULAR DISEASES; and INFECTION. With the loss of sensation and poor circulation, injuries and infections often lead to severe foot ulceration, GANGRENE and AMPUTATION. | 0 | 4.59 | 3 | 0 |
Eardrum Perforation [description not available] | 0 | 3.52 | 8 | 0 |
Tympanic Membrane Perforation A temporary or persistent opening in the eardrum (TYMPANIC MEMBRANE). Clinical signs depend on the size, location, and associated pathological condition. | 0 | 3.52 | 8 | 0 |
Cancer of the Fallopian Tube [description not available] | 0 | 4.9 | 8 | 0 |
Fallopian Tube Neoplasms Benign or malignant neoplasms of the FALLOPIAN TUBES. They are uncommon. If they develop, they may be located in the wall or within the lumen as a growth attached to the wall by a stalk. | 0 | 4.9 | 8 | 0 |
Germinoblastoma [description not available] | 0 | 8.13 | 81 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 8.13 | 81 | 0 |
Carcinoma, Medullary A carcinoma composed mainly of epithelial elements with little or no stroma. Medullary carcinomas of the breast constitute 5%-7% of all mammary carcinomas; medullary carcinomas of the thyroid comprise 3%-10% of all thyroid malignancies. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1141; Segen, Dictionary of Modern Medicine, 1992) | 0 | 6.04 | 27 | 0 |
Nodular Goiter [description not available] | 0 | 3.38 | 7 | 0 |
Goiter, Nodular An enlarged THYROID GLAND containing multiple nodules (THYROID NODULE), usually resulting from recurrent thyroid HYPERPLASIA and involution over many years to produce the irregular enlargement. Multinodular goiters may be nontoxic or may induce THYROTOXICOSIS. | 0 | 3.38 | 7 | 0 |
Dermatitis Seborrheica [description not available] | 0 | 7.65 | 20 | 2 |
Dermatitis, Seborrheic A chronic inflammatory disease of the skin with unknown etiology. It is characterized by moderate ERYTHEMA, dry, moist, or greasy (SEBACEOUS GLAND) scaling and yellow crusted patches on various areas, especially the scalp, that exfoliate as dandruff. Seborrheic dermatitis is common in children and adolescents with HIV INFECTIONS. | 0 | 7.65 | 20 | 2 |
Sterility, Male [description not available] | 0 | 3.26 | 6 | 0 |
Infertility, Male The inability of the male to effect FERTILIZATION of an OVUM after a specified period of unprotected intercourse. Male sterility is permanent infertility. | 0 | 3.26 | 6 | 0 |
Disease A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. | 0 | 6.09 | 13 | 0 |
Biliary Cirrhosis [description not available] | 0 | 4.34 | 20 | 0 |
Liver Cirrhosis, Biliary FIBROSIS of the hepatic parenchyma due to obstruction of BILE flow (CHOLESTASIS) in the intrahepatic or extrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC; BILE DUCTS, EXTRAHEPATIC). Primary biliary cholangitis involves the destruction of small intra-hepatic bile ducts and decreased bile secretion. Secondary biliary cholangitis is produced by prolonged obstruction of large intrahepatic or extrahepatic bile ducts from a variety of causes. | 0 | 4.34 | 20 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 6.56 | 27 | 0 |
Tracheal Neoplasms New abnormal growth of tissue in the TRACHEA. | 0 | 4.29 | 7 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 6.56 | 27 | 0 |
Polycystic Ovarian Syndrome [description not available] | 0 | 3.28 | 6 | 0 |
Polycystic Ovary Syndrome A complex disorder characterized by infertility, HIRSUTISM; OBESITY; and various menstrual disturbances such as OLIGOMENORRHEA; AMENORRHEA; ANOVULATION. Polycystic ovary syndrome is usually associated with bilateral enlarged ovaries studded with atretic follicles, not with cysts. The term, polycystic ovary, is misleading. | 0 | 3.28 | 6 | 0 |
Submandibular Gland Neoplasms New abnormal growth of tissue in the SUBMANDIBULAR GLAND. | 0 | 5.48 | 25 | 0 |
Liver Steatosis [description not available] | 0 | 5.36 | 13 | 0 |
Insulin Sensitivity [description not available] | 0 | 2.1 | 1 | 0 |
Fatty Liver Lipid infiltration of the hepatic parenchymal cells resulting in a yellow-colored liver. The abnormal lipid accumulation is usually in the form of TRIGLYCERIDES, either as a single large droplet or multiple small droplets. Fatty liver is caused by an imbalance in the metabolism of FATTY ACIDS. | 0 | 5.36 | 13 | 0 |
Insulin Resistance Diminished effectiveness of INSULIN in lowering blood sugar levels: requiring the use of 200 units or more of insulin per day to prevent HYPERGLYCEMIA or KETOSIS. | 0 | 2.1 | 1 | 0 |
Obesity A status with BODY WEIGHT that is grossly above the recommended standards, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY). | 0 | 4.07 | 5 | 0 |
Teeth, Devitalized [description not available] | 0 | 3.01 | 1 | 0 |
Periapical Diseases Diseases of the PERIAPICAL TISSUE surrounding the root of the tooth, which is distinguished from DENTAL PULP DISEASES inside the TOOTH ROOT. | 0 | 4.01 | 5 | 0 |
Cadaver A dead body, usually a human body. | 0 | 4.24 | 18 | 0 |
Corpus Luteum Cyst [description not available] | 0 | 3.71 | 10 | 0 |
Ovarian Cysts General term for CYSTS and cystic diseases of the OVARY. | 0 | 3.71 | 10 | 0 |
Premature Rupture of Fetal Membranes [description not available] | 0 | 2.1 | 1 | 0 |
Group A Strep Infection [description not available] | 0 | 4.62 | 10 | 0 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 2.92 | 4 | 0 |
Fetal Membranes, Premature Rupture Spontaneous tearing of the membranes surrounding the FETUS any time before the onset of OBSTETRIC LABOR. Preterm PROM is membrane rupture before 37 weeks of GESTATION. | 0 | 2.1 | 1 | 0 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 4.62 | 10 | 0 |
Adenofibroma A benign neoplasm composed of glandular and fibrous tissues, with a relatively large proportion of glands. (Stedman, 25th ed) | 0 | 5.2 | 19 | 0 |
B-Cell Lymphoma [description not available] | 0 | 3.39 | 7 | 0 |
Polyradiculitis [description not available] | 0 | 2.1 | 1 | 0 |
Polyradiculopathy Disease or injury involving multiple SPINAL NERVE ROOTS. Polyradiculitis refers to inflammation of multiple spinal nerve roots. | 0 | 2.1 | 1 | 0 |
Lymphoma, B-Cell A group of heterogeneous lymphoid tumors generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes. | 0 | 3.39 | 7 | 0 |
Parodontosis [description not available] | 0 | 9.18 | 31 | 0 |
Periodontal Diseases Pathological processes involving the PERIODONTIUM including the gum (GINGIVA), the alveolar bone (ALVEOLAR PROCESS), the DENTAL CEMENTUM, and the PERIODONTAL LIGAMENT. | 0 | 9.18 | 31 | 0 |
Dentin Hypersensitivity [description not available] | 0 | 10.33 | 15 | 11 |
Blood Loss, Postoperative [description not available] | 0 | 8.59 | 6 | 6 |
Congenital Epulides [description not available] | 0 | 6.94 | 39 | 0 |
Placenta Increta Invasion of CHORIONIC VILLI occurs deep into the MYOMETRIUM. | 0 | 2.1 | 1 | 0 |
Placenta Accreta Abnormal placentation in which all or parts of the PLACENTA are attached directly to the MYOMETRIUM due to a complete or partial absence of DECIDUA. It is associated with POSTPARTUM HEMORRHAGE because of the failure of placental separation. | 0 | 2.1 | 1 | 0 |
Middle Ear Inflammation [description not available] | 0 | 4.27 | 19 | 0 |
External Ear Inflammation [description not available] | 0 | 2.88 | 4 | 0 |
Otitis Externa Inflammation of the OUTER EAR including the external EAR CANAL, cartilages of the auricle (EAR CARTILAGE), and the TYMPANIC MEMBRANE. | 0 | 2.88 | 4 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 4.27 | 19 | 0 |
Iris Diseases Diseases, dysfunctions, or disorders of or located in the iris. | 0 | 3.6 | 9 | 0 |
Bilateral Wilms Tumor [description not available] | 0 | 6.29 | 36 | 0 |
Desmoplastic Small Cell Tumor [description not available] | 0 | 3.93 | 4 | 0 |
Wilms Tumor A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN. | 0 | 6.29 | 36 | 0 |
Desmoplastic Small Round Cell Tumor A rare, aggressive soft tissue sarcoma that primarily affects adolescents and young adults. It is most commonly found in the abdomen. | 0 | 3.93 | 4 | 0 |
Foot Dermatoses Skin diseases of the foot, general or unspecified. | 0 | 5.09 | 17 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 5.48 | 25 | 0 |
Prostatic Diseases Pathological processes involving the PROSTATE or its component tissues. | 0 | 5.63 | 18 | 0 |
Muscular Dystrophy [description not available] | 0 | 3.62 | 3 | 0 |
Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. | 0 | 3.62 | 3 | 0 |
Hypospadias A birth defect due to malformation of the URETHRA in which the urethral opening is below its normal location. In the male, the malformed urethra generally opens on the ventral surface of the PENIS or on the PERINEUM. In the female, the malformed urethral opening is in the VAGINA. | 0 | 2.94 | 4 | 0 |
Monkey Diseases Diseases of Old World and New World monkeys. This term includes diseases of baboons but not of chimpanzees or gorillas (= APE DISEASES). | 0 | 4.53 | 9 | 0 |
Acne Keloid A type of acneiform disorder in which secondary pyogenic infection in and around pilosebaceous structures ends in keloidal scarring. It manifests as persistent folliculitis of the back of the neck associated with occlusion of the follicular orifices. It is most often encountered in black or Asian men. | 0 | 2.1 | 1 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 2.1 | 1 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 2.1 | 1 | 0 |
Cystitis Inflammation of the URINARY BLADDER, either from bacterial or non-bacterial causes. Cystitis is usually associated with painful urination (dysuria), increased frequency, urgency, and suprapubic pain. | 0 | 3.37 | 7 | 0 |
Astroblastoma [description not available] | 0 | 3.29 | 6 | 0 |
Neoplasms, Neuroepithelial Neoplasms composed of neuroepithelial cells, which have the capacity to differentiate into NEURONS, oligodendrocytes, and ASTROCYTES. The majority of craniospinal tumors are of neuroepithelial origin. (From Dev Biol 1998 Aug 1;200(1):1-5) | 0 | 3.29 | 6 | 0 |
Pus [description not available] | 0 | 5.99 | 10 | 1 |
Duncan Disease [description not available] | 0 | 3.41 | 7 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 3.41 | 7 | 0 |
Cholesteatoma A non-neoplastic mass of keratin-producing squamous EPITHELIUM, frequently occurring in the MENINGES; bones of the skull, and most commonly in the MIDDLE EAR and MASTOID region. Cholesteatoma can be congenital or acquired. Cholesteatoma is not a tumor nor is it associated with high CHOLESTEROL. | 0 | 6.97 | 53 | 0 |
Airway Remodeling The structural changes in the number, mass, size and/or composition of the airway tissues. | 0 | 2.1 | 1 | 0 |
Nasal Catarrh [description not available] | 0 | 2.43 | 2 | 0 |
Sinus Infections [description not available] | 0 | 2.94 | 4 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 2.43 | 2 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 2.94 | 4 | 0 |
Embolus [description not available] | 0 | 2.42 | 2 | 0 |
Embolism Blocking of a blood vessel by an embolus which can be a blood clot or other undissolved material in the blood stream. | 0 | 2.42 | 2 | 0 |
Coloboma Congenital anomaly in which some of the structures of the eye are absent due to incomplete fusion of the fetal intraocular fissure during gestation. | 0 | 2.1 | 1 | 0 |
Complications, Pregnancy [description not available] | 0 | 3.59 | 9 | 0 |
Acute Necrotizing Pancreatitis [description not available] | 0 | 2.72 | 3 | 0 |
Osteoporotic Fractures Breaks in bones resulting from low bone mass and microarchitectural deterioration characteristic of OSTEOPOROSIS. | 0 | 2.11 | 1 | 0 |
Corneal Dystrophies [description not available] | 0 | 9.3 | 36 | 0 |
Hypertrophy General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA). | 0 | 4.28 | 19 | 0 |
Peripheral Nerve Injury [description not available] | 0 | 2.74 | 3 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 2.74 | 3 | 0 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 4.88 | 8 | 0 |
Pheochromocytoma A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298) | 0 | 4.88 | 8 | 0 |
Adult Periodontitis [description not available] | 0 | 4.46 | 2 | 2 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 2.73 | 3 | 0 |
Adenomyoepithelioma A mixed epithelial and myoepithelial neoplasm usually encountered within the breast. It is a multinodular lesion presenting with a bicellular pattern of proliferating epithelial and myoepithelial cells, which are regularly distributed in the glandular structures. | 0 | 3.42 | 2 | 0 |
Lichen Sclerosis [description not available] | 0 | 3.36 | 2 | 0 |
Lichen Sclerosus et Atrophicus A chronic inflammatory mucocutaneous disease usually affecting the female genitalia (VULVAR LICHEN SCLEROSUS) and BALANITIS XEROTICA OBLITERANS in males. It is also called white spot disease and Csillag's disease. | 0 | 3.36 | 2 | 0 |
Dysphagia [description not available] | 0 | 3.39 | 7 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 3.96 | 13 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 2.69 | 3 | 0 |
Deglutition Disorders Difficulty in SWALLOWING which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the PHARYNX and UPPER ESOPHAGEAL SPHINCTER; and esophageal dysphagia due to malfunction of the ESOPHAGUS. | 0 | 3.39 | 7 | 0 |
Monilethrix Rare autosomal dominant disorder of the hair shaft. The clinical features of the disease include HYPOTRICHOSIS, dry, and/or brittle hair, with varying degrees of ALOPECIA. Mutations in the hair-specific keratin genes KRTHB1, KRTHB3, or KRTHB6 are associated with monilethrix. Autosomal recessive monilethrix with limited HYPOTRICHOSIS are also known. Mutations in Dsg4, Liph, and P2ry5 protein genes are associated with the recessive form of monilethrix. | 0 | 2.68 | 3 | 0 |
Tooth Mobility Horizontal and, to a lesser degree, axial movement of a tooth in response to normal forces, as in occlusion. It refers also to the movability of a tooth resulting from loss of all or a portion of its attachment and supportive apparatus, as seen in periodontitis, occlusal trauma, and periodontosis. (From Jablonski, Dictionary of Dentistry, 1992, p507 & Boucher's Clinical Dental Terminology, 4th ed, p313) | 0 | 8.32 | 7 | 5 |
Microsatellite Instability The occurrence of highly polymorphic mono- and dinucleotide MICROSATELLITE REPEATS in somatic cells. It is a form of genome instability associated with defects in DNA MISMATCH REPAIR. | 0 | 2.75 | 3 | 0 |
Mouth Ulcer [description not available] | 0 | 4.43 | 8 | 0 |
Deficiency, Mental [description not available] | 0 | 4.59 | 10 | 0 |
Intellectual Disability Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28) | 0 | 4.59 | 10 | 0 |
Oral Ulcer A loss of mucous substance of the mouth showing local excavation of the surface, resulting from the sloughing of inflammatory necrotic tissue. It is the result of a variety of causes, e.g., denture irritation, aphthous stomatitis (STOMATITIS, APHTHOUS); NOMA; necrotizing gingivitis (GINGIVITIS, NECROTIZING ULCERATIVE); TOOTHBRUSHING; and various irritants. (From Jablonski, Dictionary of Dentistry, 1992, p842) | 0 | 4.43 | 8 | 0 |
Cancer of Pelvis [description not available] | 0 | 3.78 | 11 | 0 |
Complications of Diabetes Mellitus [description not available] | 0 | 2.92 | 4 | 0 |
Papilloma, Intraductal A small, often impalpable benign papilloma arising in a lactiferous duct and frequently causing bleeding from the nipple. (Stedman, 25th ed) | 0 | 3.8 | 11 | 0 |
Benign Fibrous Mesothelioma [description not available] | 0 | 2.52 | 2 | 0 |
Cocaine Abuse [description not available] | 0 | 2.13 | 1 | 0 |
Cocaine-Related Disorders Disorders related or resulting from use of cocaine. | 0 | 2.13 | 1 | 0 |
Bone Cysts Benign unilocular lytic areas in the proximal end of a long bone with well defined and narrow endosteal margins. The cysts contain fluid and the cyst walls may contain some giant cells. Bone cysts usually occur in males between the ages 3-15 years. | 0 | 3.57 | 9 | 0 |
Gangliocytoma [description not available] | 0 | 4.33 | 7 | 0 |
Connective Tissue Neoplasms [description not available] | 0 | 3.63 | 3 | 0 |
Fasciola Infection [description not available] | 0 | 2.11 | 1 | 0 |
Fascioliasis Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA. | 0 | 2.11 | 1 | 0 |
Adenoma, Adrenal Cortical [description not available] | 0 | 3.42 | 2 | 0 |
Rodent Diseases Diseases of rodents of the order RODENTIA. This term includes diseases of Sciuridae (squirrels), Geomyidae (gophers), Heteromyidae (pouched mice), Castoridae (beavers), Cricetidae (rats and mice), Muridae (Old World rats and mice), Erethizontidae (porcupines), and Caviidae (guinea pigs). | 0 | 5.05 | 16 | 0 |
Berger Disease [description not available] | 0 | 2.73 | 3 | 0 |
Glomerulonephritis, IGA A chronic form of glomerulonephritis characterized by deposits of predominantly IMMUNOGLOBULIN A in the mesangial area (GLOMERULAR MESANGIUM). Deposits of COMPLEMENT C3 and IMMUNOGLOBULIN G are also often found. Clinical features may progress from asymptomatic HEMATURIA to END-STAGE KIDNEY DISEASE. | 0 | 2.73 | 3 | 0 |
Disseminated Fusariosis [description not available] | 0 | 2.11 | 1 | 0 |
Fusariosis OPPORTUNISTIC INFECTIONS with the soil fungus FUSARIUM. Typically the infection is limited to the nail plate (ONYCHOMYCOSIS). The infection can however become systemic especially in an IMMUNOCOMPROMISED HOST (e.g., NEUTROPENIA) and results in cutaneous and subcutaneous lesions, fever, KERATITIS, and pulmonary infections. | 0 | 2.11 | 1 | 0 |
(pPNET) Peripheral Primitive Neuroectodermal Tumors [description not available] | 0 | 4.84 | 13 | 0 |
Neuroectodermal Tumors, Primitive, Peripheral A group of highly cellular primitive round cell neoplasms which occur extracranially in soft tissue and bone and are derived from embryonal neural crest cells. These tumors occur primarily in children and adolescents and share a number of characteristics with EWING SARCOMA. | 0 | 4.84 | 13 | 0 |
Chronic Esophagitis, Eosinophilic [description not available] | 0 | 3.88 | 2 | 1 |
Eosinophilic Esophagitis Chronic ESOPHAGITIS characterized by esophageal mucosal EOSINOPHILIA. It is diagnosed when an increase in EOSINOPHILS are present over the entire esophagus. The reflux symptoms fail to respond to PROTON PUMP INHIBITORS treatment, unlike in GASTROESOPHAGEAL REFLUX DISEASE. The symptoms are associated with IgE-mediated hypersensitivity to food or inhalant allergens. | 0 | 3.88 | 2 | 1 |
Nevi, Spindle Cell [description not available] | 0 | 2.11 | 1 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 3.96 | 1 | 0 |
Foot Ulcer Lesion on the surface of the skin of the foot, usually accompanied by inflammation. The lesion may become infected or necrotic and is frequently associated with diabetes or leprosy. | 0 | 4.56 | 3 | 0 |
Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325) | 0 | 3.96 | 1 | 0 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 3.82 | 2 | 1 |
Bacterial Eye Infections [description not available] | 0 | 2.52 | 2 | 0 |
Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | 0 | 3.82 | 2 | 1 |
Jaw, Edentulous, Partially Absence of teeth from a portion of the mandible and/or maxilla. | 0 | 4.08 | 3 | 1 |
Adenoma, Prostatic [description not available] | 0 | 10.07 | 91 | 2 |
Prostatic Hyperplasia Increase in constituent cells in the PROSTATE, leading to enlargement of the organ (hypertrophy) and adverse impact on the lower urinary tract function. This can be caused by increased rate of cell proliferation, reduced rate of cell death, or both. | 0 | 10.07 | 91 | 2 |
Bilateral Nasal Obstruction [description not available] | 0 | 2.73 | 3 | 0 |
Nasal Obstruction Any hindrance to the passage of air into and out of the nose. The obstruction may be unilateral or bilateral, and may involve any part of the NASAL CAVITY. | 0 | 2.73 | 3 | 0 |
Thyroid Nodule A small circumscribed mass in the THYROID GLAND that can be of neoplastic growth or non-neoplastic abnormality. It lacks a well-defined capsule or glandular architecture. Thyroid nodules are often benign but can be malignant. The growth of nodules can lead to a multinodular goiter (GOITER, NODULAR). | 0 | 5.49 | 15 | 0 |
Gingival Hyperplasia Non-inflammatory enlargement of the gingivae produced by factors other than local irritation. It is characteristically due to an increase in the number of cells. (From Jablonski's Dictionary of Dentistry, 1992, p400) | 0 | 3.06 | 5 | 0 |
Acinar Carcinoma [description not available] | 0 | 5.28 | 20 | 0 |
Carcinoma, Acinar Cell A malignant tumor arising from secreting cells of a racemose gland, particularly the salivary glands. Racemose (Latin racemosus, full of clusters) refers, as does acinar (Latin acinus, grape), to small saclike dilatations in various glands. Acinar cell carcinomas are usually well differentiated and account for about 13% of the cancers arising in the parotid gland. Lymph node metastasis occurs in about 16% of cases. Local recurrences and distant metastases many years after treatment are common. This tumor appears in all age groups and is most common in women. (Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1240; from DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p575) | 0 | 5.28 | 20 | 0 |
Neisseria gonorrhoeae Infection [description not available] | 0 | 2.45 | 2 | 0 |
Corneal Perforation A puncture or hole through the CORNEAL STROMA resulting from various diseases or trauma. | 0 | 2.11 | 1 | 0 |
Gonorrhea Acute infectious disease characterized by primary invasion of the urogenital tract. The etiologic agent, NEISSERIA GONORRHOEAE, was isolated by Neisser in 1879. | 0 | 2.45 | 2 | 0 |
Acute Renal Colic [description not available] | 0 | 2.11 | 1 | 0 |
Renal Colic A severe intermittent and spasmodic pain in the lower back radiating to the groin, scrotum, and labia which is most commonly caused by a kidney stone (RENAL CALCULUS) passing through the URETER or by other urinary track blockage. It is often associated with nausea, vomiting, fever, restlessness, dull pain, frequent urination, and HEMATURIA. | 0 | 2.11 | 1 | 0 |
Apocrine Poroma Benign adnexal neoplasm whose glandular secretion includes the release of part of the secreting cell. | 0 | 2.48 | 2 | 0 |
Mesonephroma A rare tumor of the female genital tract, most often the ovary, formerly considered to be derived from mesonephric rests. Two varieties are recognized: (1) clear cell carcinoma, so called because of its histologic resemblance to renal cell carcinoma, and now considered to be of muellerian duct derivation and (2) an embryonal tumor (called also ENDODERMAL SINUS TUMOR and yolk sac tumor), occurring chiefly in children. The latter variety may also arise in the testis. (Dorland, 27th ed) | 0 | 5.8 | 22 | 0 |
Genital Diseases, Male Pathological processes involving the male reproductive tract (GENITALIA, MALE). | 0 | 3.79 | 11 | 0 |
Focal Segmental Glomerulosclerosis [description not available] | 0 | 2.95 | 4 | 0 |
Glomerulosclerosis, Focal Segmental A clinicopathological syndrome or diagnostic term for a type of glomerular injury that has multiple causes, primary or secondary. Clinical features include PROTEINURIA, reduced GLOMERULAR FILTRATION RATE, and EDEMA. Kidney biopsy initially indicates focal segmental glomerular consolidation (hyalinosis) or scarring which can progress to globally sclerotic glomeruli leading to eventual KIDNEY FAILURE. | 0 | 2.95 | 4 | 0 |
Bronchopulmonary Dysplasia A chronic lung disease developed after OXYGEN INHALATION THERAPY or mechanical ventilation (VENTILATION, MECHANICAL) usually occurring in certain premature infants (INFANT, PREMATURE) or newborn infants with respiratory distress syndrome (RESPIRATORY DISTRESS SYNDROME, NEWBORN). Histologically, it is characterized by the unusual abnormalities of the bronchioles, such as METAPLASIA, decrease in alveolar number, and formation of CYSTS. | 0 | 2.47 | 2 | 0 |
Limb-Girdle Muscular Dystrophies [description not available] | 0 | 2.11 | 1 | 0 |
Muscular Dystrophies, Limb-Girdle A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles). | 0 | 2.11 | 1 | 0 |
Abnormality, Heart [description not available] | 0 | 2.92 | 4 | 0 |
Heart Defects, Congenital Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life. | 0 | 2.92 | 4 | 0 |
American Trypanosomiasis [description not available] | 0 | 2.11 | 1 | 0 |
Chagas Disease Infection with the protozoan parasite TRYPANOSOMA CRUZI, a form of TRYPANOSOMIASIS endemic in Central and South America. It is named after the Brazilian physician Carlos Chagas, who discovered the parasite. Infection by the parasite (positive serologic result only) is distinguished from the clinical manifestations that develop years later, such as destruction of PARASYMPATHETIC GANGLIA; CHAGAS CARDIOMYOPATHY; and dysfunction of the ESOPHAGUS or COLON. | 0 | 2.11 | 1 | 0 |
Laryngeal Diseases Pathological processes involving any part of the LARYNX which coordinates many functions such as voice production, breathing, swallowing, and coughing. | 0 | 3.61 | 9 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 5.52 | 16 | 0 |
Astrocytoma Neoplasms of the brain and spinal cord derived from glial cells which vary from histologically benign forms to highly anaplastic and malignant tumors. Fibrillary astrocytomas are the most common type and may be classified in order of increasing malignancy (grades I through IV). In the first two decades of life, astrocytomas tend to originate in the cerebellar hemispheres; in adults, they most frequently arise in the cerebrum and frequently undergo malignant transformation. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2013-7; Holland et al., Cancer Medicine, 3d ed, p1082) | 0 | 5.52 | 16 | 0 |
Acute Autoimmune Neuropathy [description not available] | 0 | 2.48 | 2 | 0 |
Guillain-Barre Syndrome An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (From Adams et al., Principles of Neurology, 6th ed, pp1312-1314) | 0 | 2.48 | 2 | 0 |
Papulosquamous Disorders [description not available] | 0 | 3.11 | 5 | 0 |
Acneiform Eruptions Visible efflorescent lesions of the skin caused by acne or resembling acne. (Dorland, 28th ed, p18, 575) | 0 | 2.13 | 1 | 0 |
46, XX Disorders of Sex Development Congenital conditions in individuals with a female karyotype, in which the development of the gonadal or anatomical sex is atypical. | 0 | 2.15 | 1 | 0 |
Carcinoma, Large Cell A tumor of undifferentiated (anaplastic) cells of large size. It is usually bronchogenic. (From Dorland, 27th ed) | 0 | 6.59 | 27 | 0 |
Astrocytosis [description not available] | 0 | 2.69 | 3 | 0 |
Allodynia [description not available] | 0 | 2.9 | 4 | 0 |
Nerve Pain [description not available] | 0 | 2.13 | 1 | 0 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 2.13 | 1 | 0 |
Dermatitis, Radiation-Induced [description not available] | 0 | 2.67 | 3 | 0 |
Radiodermatitis A cutaneous inflammatory reaction occurring as a result of exposure to ionizing radiation. | 0 | 2.67 | 3 | 0 |
Mandibular Diseases Diseases involving the MANDIBLE. | 0 | 8.32 | 70 | 0 |
Malaria, Avian Any of a group of infections of fowl caused by protozoa of the genera PLASMODIUM, Leucocytozoon, and Haemoproteus. The life cycles of these parasites and the disease produced bears strong resemblance to those observed in human malaria. | 0 | 2.13 | 1 | 0 |
Dental Wear [description not available] | 0 | 2.13 | 1 | 0 |
Meigs Syndrome The triad of benign FIBROMA or other ovarian tumors with ASCITES, and HYDROTHORAX due to large PLEURAL EFFUSIONS. | 0 | 3.04 | 1 | 0 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 3.36 | 2 | 0 |
Lichen Ruber Planus [description not available] | 0 | 8.51 | 55 | 1 |
Lichen Planus An inflammatory, pruritic disease of the skin and mucous membranes, which can be either generalized or localized. It is characterized by distinctive purplish, flat-topped papules having a predilection for the trunk and flexor surfaces. The lesions may be discrete or coalesce to form plaques. Histologically, there is a saw-tooth pattern of epidermal hyperplasia and vacuolar alteration of the basal layer of the epidermis along with an intense upper dermal inflammatory infiltrate composed predominantly of T-cells. Etiology is unknown. | 0 | 8.51 | 55 | 1 |
Ureteral Obstruction Blockage in any part of the URETER causing obstruction of urine flow from the kidney to the URINARY BLADDER. The obstruction may be congenital, acquired, unilateral, bilateral, complete, partial, acute, or chronic. Depending on the degree and duration of the obstruction, clinical features vary greatly such as HYDRONEPHROSIS and obstructive nephropathy. | 0 | 2.71 | 3 | 0 |
Vaginal Diseases Pathological processes of the VAGINA. | 0 | 4.5 | 9 | 0 |
Angle's Classification [description not available] | 0 | 2.41 | 2 | 0 |
Malocclusion Such malposition and contact of the maxillary and mandibular teeth as to interfere with the highest efficiency during the excursive movements of the jaw that are essential for mastication. (Jablonski, Illustrated Dictionary of Dentistry, 1982) | 0 | 2.41 | 2 | 0 |
Gasser Syndrome [description not available] | 0 | 2.13 | 1 | 0 |
Hemolytic-Uremic Syndrome A syndrome that is associated with microvascular diseases of the KIDNEY, such as RENAL CORTICAL NECROSIS. It is characterized by hemolytic anemia (ANEMIA, HEMOLYTIC); THROMBOCYTOPENIA; and ACUTE RENAL FAILURE. | 0 | 2.13 | 1 | 0 |
Pneumonia, Pneumococcal A febrile disease caused by STREPTOCOCCUS PNEUMONIAE. | 0 | 3.42 | 2 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 5.62 | 18 | 1 |
Ambulation Disorders, Neurologic [description not available] | 0 | 2.13 | 1 | 0 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 2.43 | 2 | 0 |
Neoplasms, Skull Base [description not available] | 0 | 5.48 | 9 | 0 |
Enterovirus Infections Diseases caused by ENTEROVIRUS. | 0 | 2.13 | 1 | 0 |
Follicular Thyroid Carcinoma [description not available] | 0 | 5.37 | 22 | 0 |
Adenocarcinoma, Follicular An adenocarcinoma of the thyroid gland, in which the cells are arranged in the form of follicles. (From Dorland, 27th ed) | 0 | 5.37 | 22 | 0 |
Muscle Tissue Neoplasms [description not available] | 0 | 5.51 | 16 | 0 |
Nasal Bleeding [description not available] | 0 | 2.13 | 1 | 0 |
Epistaxis Bleeding from the nose. | 0 | 2.13 | 1 | 0 |
Amelogenesis Imperfecta A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION. | 0 | 2.13 | 1 | 0 |
Blood Pressure, High [description not available] | 0 | 3.11 | 5 | 0 |
Hypertension Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more. | 0 | 3.11 | 5 | 0 |
Infection, Wound [description not available] | 0 | 2.42 | 2 | 0 |
Brain Swelling [description not available] | 0 | 4.51 | 5 | 1 |
Absence Seizure [description not available] | 0 | 2.67 | 3 | 0 |
Brain Edema Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see HYPOXIA, BRAIN). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of CSF flow (e.g., obstructive HYDROCEPHALUS). (From Childs Nerv Syst 1992 Sep; 8(6):301-6) | 0 | 4.51 | 5 | 1 |
Seizures Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder. | 0 | 2.67 | 3 | 0 |
Black Fever [description not available] | 0 | 2.48 | 2 | 0 |
Leishmaniasis, Visceral A chronic disease caused by LEISHMANIA DONOVANI and transmitted by the bite of several sandflies of the genera Phlebotomus and Lutzomyia. It is commonly characterized by fever, chills, vomiting, anemia, hepatosplenomegaly, leukopenia, hypergammaglobulinemia, emaciation, and an earth-gray color of the skin. The disease is classified into three main types according to geographic distribution: Indian, Mediterranean (or infantile), and African. | 0 | 2.48 | 2 | 0 |
Pancreatic Cyst A true cyst of the PANCREAS, distinguished from the much more common PANCREATIC PSEUDOCYST by possessing a lining of mucous EPITHELIUM. Pancreatic cysts are categorized as congenital, retention, neoplastic, parasitic, enterogenous, or dermoid. Congenital cysts occur more frequently as solitary cysts but may be multiple. Retention cysts are gross enlargements of PANCREATIC DUCTS secondary to ductal obstruction. (From Bockus Gastroenterology, 4th ed, p4145) | 0 | 5.31 | 9 | 0 |
Microphthalmia [description not available] | 0 | 2.71 | 3 | 0 |
Hydronephrosis Abnormal enlargement or swelling of a KIDNEY due to dilation of the KIDNEY CALICES and the KIDNEY PELVIS. It is often associated with obstruction of the URETER or chronic kidney diseases that prevents normal drainage of urine into the URINARY BLADDER. | 0 | 2.13 | 1 | 0 |
Pleural Effusion Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. It is a sign of disease and not a diagnosis in itself. | 0 | 5.12 | 45 | 0 |
Infections, Picornaviridae [description not available] | 0 | 2.13 | 1 | 0 |
Adenoma, Oxyphilic A usually benign glandular tumor composed of oxyphil cells, large cells with small irregular nuclei and dense acidophilic granules due to the presence of abundant MITOCHONDRIA. Oxyphil cells, also known as oncocytes, are found in oncocytomas of the kidney, salivary glands, and endocrine glands. In the thyroid gland, oxyphil cells are known as Hurthle cells and Askanazy cells. | 0 | 8.34 | 39 | 1 |
Carotid Artery Narrowing [description not available] | 0 | 2.13 | 1 | 0 |
Carotid Stenosis Narrowing or stricture of any part of the CAROTID ARTERIES, most often due to atherosclerotic plaque formation. Ulcerations may form in atherosclerotic plaques and induce THROMBUS formation. Platelet or cholesterol emboli may arise from stenotic carotid lesions and induce a TRANSIENT ISCHEMIC ATTACK; CEREBROVASCULAR ACCIDENT; or temporary blindness (AMAUROSIS FUGAX). (From Adams et al., Principles of Neurology, 6th ed, pp 822-3) | 0 | 2.13 | 1 | 0 |
Cystic Kidney Diseases [description not available] | 0 | 4.31 | 7 | 0 |
Kidney Diseases, Cystic A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC). | 0 | 4.31 | 7 | 0 |
Cell Transformation, Viral An inheritable change in cells manifested by changes in cell division and growth and alterations in cell surface properties. It is induced by infection with a transforming virus. | 0 | 7.39 | 111 | 0 |
Yolk Sac Tumor [description not available] | 0 | 4.63 | 10 | 0 |
Endodermal Sinus Tumor An unusual and aggressive tumor of germ-cell origin that reproduces the extraembryonic structures of the early embryo. It is the most common malignant germ cell tumor found in children. It is characterized by a labyrinthine glandular pattern of flat epithelial cells and rounded papillary processes with a central capillary (Schiller-Duval body). The tumor is rarely bilateral. Before the use of combination chemotherapy, the tumor was almost invariably fatal. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1189) | 0 | 4.63 | 10 | 0 |
B-K Mole Syndrome [description not available] | 0 | 2.15 | 1 | 0 |
Dysplastic Nevus Syndrome Clinically atypical nevi (usually exceeding 5 mm in diameter and having variable pigmentation and ill defined borders) with an increased risk for development of non-familial cutaneous malignant melanoma. Biopsies show melanocytic dysplasia. Nevi are clinically and histologically identical to the precursor lesions for melanoma in the B-K mole syndrome. (Stedman, 25th ed) | 0 | 2.15 | 1 | 0 |
Neuroma A tumor made up of nerve cells and nerve fibers. (Dorland, 27th ed) | 0 | 2.15 | 1 | 0 |
Albright Syndrome [description not available] | 0 | 2.15 | 1 | 0 |
Femoral Neoplasms New abnormal growth of tissue in the FEMUR. | 0 | 2.7 | 3 | 0 |
Fibrous Dysplasia, Polyostotic FIBROUS DYSPLASIA OF BONE affecting several bones. When melanotic pigmentation (CAFE-AU-LAIT SPOTS) and multiple endocrine hyperfunction are additionally associated it is referred to as Albright syndrome. | 0 | 2.15 | 1 | 0 |
Acute-On-Chronic Liver Failure (ACLF) [description not available] | 0 | 2.13 | 1 | 0 |
Acute-On-Chronic Liver Failure Sudden liver failure in the presence of underlying compensated chronic LIVER DISEASE (e.g., LIVER CIRRHOSIS; HEPATITIS; and liver injury and failure) due to a precipitating acute hepatic insult. | 0 | 2.13 | 1 | 0 |
Tetraploid [description not available] | 0 | 2.15 | 1 | 0 |
Disbacteriosis [description not available] | 0 | 2.15 | 1 | 0 |
Cancer of Gallbladder [description not available] | 0 | 7.54 | 31 | 1 |
Gallbladder Neoplasms Tumors or cancer of the gallbladder. | 0 | 7.54 | 31 | 1 |
Electron Transport Chain Deficiencies, Mitochondrial [description not available] | 0 | 3.39 | 2 | 0 |
Cochlear Hearing Loss [description not available] | 0 | 2.92 | 4 | 0 |
Hearing Loss, Sensorineural Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM. | 0 | 2.92 | 4 | 0 |
Mitochondrial Diseases Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. | 0 | 3.39 | 2 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 2.15 | 1 | 0 |
Renal Insufficiency, Chronic Conditions in which the KIDNEYS perform below the normal level for more than three months. Chronic kidney insufficiency is classified by five stages according to the decline in GLOMERULAR FILTRATION RATE and the degree of kidney damage (as measured by the level of PROTEINURIA). The most severe form is the end-stage renal disease (CHRONIC KIDNEY FAILURE). (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002) | 0 | 2.15 | 1 | 0 |
Nephrolithiasis Formation of stones in the KIDNEY. | 0 | 2.49 | 2 | 0 |
Sebaceous Gland Diseases Diseases of the sebaceous glands such as sebaceous hyperplasia and sebaceous cell carcinoma (SEBACEOUS GLAND NEOPLASMS). | 0 | 3.3 | 6 | 0 |
Kaposi Sarcoma [description not available] | 0 | 2.7 | 3 | 0 |
Sarcoma, Kaposi A multicentric, malignant neoplastic vascular proliferation characterized by the development of bluish-red cutaneous nodules, usually on the lower extremities, most often on the toes or feet, and slowly increasing in size and number and spreading to more proximal areas. The tumors have endothelium-lined channels and vascular spaces admixed with variably sized aggregates of spindle-shaped cells, and often remain confined to the skin and subcutaneous tissue, but widespread visceral involvement may occur. Kaposi's sarcoma occurs spontaneously in Jewish and Italian males in Europe and the United States. An aggressive variant in young children is endemic in some areas of Africa. A third form occurs in about 0.04% of kidney transplant patients. There is also a high incidence in AIDS patients. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, pp2105-7) HHV-8 is the suspected cause. | 0 | 2.7 | 3 | 0 |
Cancer of Larynx [description not available] | 0 | 7.86 | 83 | 0 |
Laryngeal Neoplasms Cancers or tumors of the LARYNX or any of its parts: the GLOTTIS; EPIGLOTTIS; LARYNGEAL CARTILAGES; LARYNGEAL MUSCLES; and VOCAL CORDS. | 0 | 7.86 | 83 | 0 |
Cancer of the Ureter [description not available] | 0 | 4.8 | 12 | 0 |
Ureteral Neoplasms Cancer or tumors of the URETER which may cause obstruction leading to hydroureter, HYDRONEPHROSIS, and PYELONEPHRITIS. HEMATURIA is a common symptom. | 0 | 4.8 | 12 | 0 |
Cystadenocarcinoma, Serous A malignant cystic or semicystic neoplasm. It often occurs in the ovary and usually bilaterally. The external surface is usually covered with papillary excrescences. Microscopically, the papillary patterns are predominantly epithelial overgrowths with differentiated and undifferentiated papillary serous cystadenocarcinoma cells. Psammoma bodies may be present. The tumor generally adheres to surrounding structures and produces ascites. (From Hughes, Obstetric-Gynecologic Terminology, 1972, p185) | 0 | 4.04 | 14 | 0 |
Carcinoma, Papillary, Follicular A thyroid neoplasm of mixed papillary and follicular arrangement. Its biological behavior and prognosis is the same as that of a papillary adenocarcinoma of the thyroid. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1271) | 0 | 4.64 | 10 | 0 |
Angioma, Sclerosing [description not available] | 0 | 6.15 | 31 | 0 |
Histiocytoma, Benign Fibrous A benign tumor composed, wholly or in part, of cells with the morphologic characteristics of HISTIOCYTES and with various fibroblastic components. Fibrous histiocytomas can occur anywhere in the body. When they occur in the skin, they are called dermatofibromas or sclerosing hemangiomas. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 5th ed, p1747) | 0 | 6.15 | 31 | 0 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 5.2 | 19 | 0 |
Myasthenia Gravis A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition. | 0 | 5.2 | 19 | 0 |
Adenoma, Sweat Gland A benign neoplasm derived from epithelial cells of sweat glands. (Stedman, 25th ed) | 0 | 6.69 | 54 | 0 |
Furcation Defects Conditions in which a bifurcation or trifurcation of the molar tooth root becomes denuded as a result of periodontal disease. It may be followed by tooth mobility, temperature sensitivity, pain, and alveolar bone resorption. | 0 | 3.38 | 2 | 0 |
Centriacinar Emphysema [description not available] | 0 | 2.7 | 3 | 0 |
Cyst, Dental Root [description not available] | 0 | 3.35 | 7 | 0 |
Adenoma Sebaceum Facial ANGIOFIBROMA in tuberous sclerosis | 0 | 5.48 | 11 | 0 |
Multiple Pulmonary Nodules A number of small lung lesions characterized by small round masses of 2- to 3-mm in diameter. They are usually detected by chest CT scans (COMPUTED TOMOGRAPHY, X-RAY). Such nodules can be associated with metastases of malignancies inside or outside the lung, benign granulomas, or other lesions. | 0 | 2.04 | 1 | 0 |
Tuberous Sclerosis Autosomal dominant neurocutaneous syndrome classically characterized by MENTAL RETARDATION; EPILEPSY; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). There is, however, considerable heterogeneity in the neurologic manifestations. It is also associated with cortical tuber and HAMARTOMAS formation throughout the body, especially the heart, kidneys, and eyes. Mutations in two loci TSC1 and TSC2 that encode hamartin and tuberin, respectively, are associated with the disease. | 0 | 5.48 | 11 | 0 |
Melanoameloblastoma [description not available] | 0 | 4.05 | 5 | 0 |
Neoplasm Seeding The local implantation of tumor cells by contamination of instruments and surgical equipment during and after surgical resection, resulting in local growth of the cells and tumor formation. | 0 | 6.1 | 11 | 1 |
Precordial Catch [description not available] | 0 | 2.96 | 1 | 0 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 2.96 | 1 | 0 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 2.96 | 1 | 0 |
Acute Respiratory Distress Syndrome [description not available] | 0 | 2.44 | 2 | 0 |
Respiratory Distress Syndrome A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA. | 0 | 2.44 | 2 | 0 |
Embryopathies [description not available] | 0 | 4.98 | 15 | 0 |
Infections, Retroviridae [description not available] | 0 | 2.45 | 2 | 0 |
Retroviridae Infections Virus diseases caused by the RETROVIRIDAE. | 0 | 2.45 | 2 | 0 |
Middle Ear Effusion [description not available] | 0 | 2.71 | 3 | 0 |
Otitis Media with Effusion Inflammation of the middle ear with a clear pale yellow-colored transudate. | 0 | 2.71 | 3 | 0 |
Bernard Syndrome [description not available] | 0 | 2.42 | 2 | 0 |
HIV Coinfection [description not available] | 0 | 5.59 | 17 | 0 |
HIV Infections Includes the spectrum of human immunodeficiency virus infections that range from asymptomatic seropositivity, thru AIDS-related complex (ARC), to acquired immunodeficiency syndrome (AIDS). | 0 | 5.59 | 17 | 0 |
Cushing's Syndrome [description not available] | 0 | 4.48 | 5 | 0 |
Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. | 0 | 4.48 | 5 | 0 |
Neoplasms, Bone Marrow [description not available] | 0 | 12.67 | 82 | 7 |
Bone Marrow Neoplasms Neoplasms located in the bone marrow. They are differentiated from neoplasms composed of bone marrow cells, such as MULTIPLE MYELOMA. Most bone marrow neoplasms are metastatic. | 0 | 12.67 | 82 | 7 |
Hematuria Presence of blood in the urine. | 0 | 5.67 | 10 | 0 |
Mastitis, Bovine INFLAMMATION of the UDDER in cows. | 0 | 5.31 | 13 | 0 |
Cervix Diseases [description not available] | 0 | 3.69 | 10 | 0 |
Gall Bladder Diseases [description not available] | 0 | 4 | 5 | 0 |
Cataract, Membranous [description not available] | 0 | 5.91 | 9 | 1 |
Cataract Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed) | 0 | 5.91 | 9 | 1 |
Female Genital Neoplasms [description not available] | 0 | 6.53 | 26 | 0 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 2.44 | 2 | 0 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 6.53 | 26 | 0 |
Libman-Sacks Disease [description not available] | 0 | 4.97 | 15 | 0 |
Lupus Erythematosus, Systemic A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. | 0 | 4.97 | 15 | 0 |
Cystadenocarcinoma, Mucinous A malignant cystic or semisolid tumor most often occurring in the ovary. Rarely, one is solid. This tumor may develop from a mucinous cystadenoma, or it may be malignant at the onset. The cysts are lined with tall columnar epithelial cells; in others, the epithelium consists of many layers of cells that have lost normal structure entirely. In the more undifferentiated tumors, one may see sheets and nests of tumor cells that have very little resemblance to the parent structure. (Hughes, Obstetric-Gynecologic Terminology, 1972, p184) | 0 | 5.59 | 17 | 0 |
Cystadenoma, Mucinous A multilocular tumor with mucin secreting epithelium. They are most often found in the ovary, but are also found in the pancreas, appendix, and rarely, retroperitoneal and in the urinary bladder. They are considered to have low-grade malignant potential. | 0 | 3.11 | 5 | 0 |
Retroperitoneal Neoplasms New abnormal growth of tissue in the RETROPERITONEAL SPACE. | 0 | 5.48 | 15 | 0 |
Multiple Neurofibromas [description not available] | 0 | 2.96 | 1 | 0 |
Aura [description not available] | 0 | 3.59 | 3 | 0 |
Epilepsy A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) | 0 | 3.59 | 3 | 0 |
Neurofibromatoses A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72) | 0 | 2.96 | 1 | 0 |
CD4-Positive T-Lymphocytopenia, Idiopathic [description not available] | 0 | 2.05 | 1 | 0 |
T-Lymphocytopenia, Idiopathic CD4-Positive Reproducible depletion of CD4+ lymphocytes below 300 per cubic millimeter in the absence of HIV infection or other known causes of immunodeficiency. This is a rare, heterogeneous syndrome and does not appear to be caused by a transmissible agent. | 0 | 2.05 | 1 | 0 |
Calculosis [description not available] | 0 | 2.43 | 2 | 0 |
Mammary Paget Disease [description not available] | 0 | 5.5 | 26 | 0 |
Experimental Leukemia [description not available] | 0 | 2.05 | 1 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 5.94 | 25 | 1 |
Chondroma A benign neoplasm derived from mesodermal cells that form cartilage. It may remain within the substance of a cartilage or bone (true chondroma or enchondroma) or may develop on the surface of a cartilage (ecchondroma or ecchondrosis). (Dorland, 27th ed; Stedman, 25th ed) | 0 | 5.06 | 7 | 0 |
Aortic Incompetence [description not available] | 0 | 2.05 | 1 | 0 |
Eccentro-Osteochondrodysplasia [description not available] | 0 | 4.85 | 8 | 1 |
Aortic Valve Insufficiency Pathological condition characterized by the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to regurgitation. It is caused by diseases of the AORTIC VALVE or its surrounding tissue (aortic root). | 0 | 2.05 | 1 | 0 |
Mucopolysaccharidosis IV Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme. | 0 | 4.85 | 8 | 1 |
Cancer of Endocrine Gland [description not available] | 0 | 5.05 | 5 | 0 |
Endocrine Gland Neoplasms Tumors or cancer of the ENDOCRINE GLANDS. | 0 | 5.05 | 5 | 0 |
Inflammatory Pseudotumor [description not available] | 0 | 5.32 | 9 | 0 |
Granuloma, Plasma Cell A slow-growing benign pseudotumor in which plasma cells greatly outnumber the inflammatory cells. | 0 | 5.32 | 9 | 0 |
Branchial Cleft Cyst [description not available] | 0 | 2.92 | 4 | 0 |
Infections, Staphylococcal Skin [description not available] | 0 | 2.92 | 4 | 0 |
Pyoderma Any purulent skin disease (Dorland, 27th ed). | 0 | 2.46 | 2 | 0 |
Staphylococcal Skin Infections Infections to the skin caused by bacteria of the genus STAPHYLOCOCCUS. | 0 | 2.92 | 4 | 0 |
Eye Burns Injury to any part of the eye by extreme heat, chemical agents, or ultraviolet radiation. | 0 | 4.41 | 8 | 0 |
EBV Infections [description not available] | 0 | 3.64 | 9 | 0 |
B Virus Infection [description not available] | 0 | 4.4 | 8 | 0 |
Immunoblastic Large-Cell Lymphoma [description not available] | 0 | 2.05 | 1 | 0 |
Epstein-Barr Virus Infections Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY). | 0 | 3.64 | 9 | 0 |
Complications, Neoplastic Pregnancy [description not available] | 0 | 4.78 | 7 | 0 |
Idiopathic Inflammatory Myopathies [description not available] | 0 | 2.05 | 1 | 0 |
Myositis Inflammation of a muscle or muscle tissue. | 0 | 2.05 | 1 | 0 |
Angiolipoma A benign neoplasm composed of a mixture of adipose tissue and blood vessels. (Dorland, 27th ed) | 0 | 2.05 | 1 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 3.94 | 13 | 0 |
Hepatitis B INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 3.94 | 13 | 0 |
Chondrodysplasia Punctata A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC), an autosomal dominant form (Conradi-Hunermann syndrome), and a milder X-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form. | 0 | 2.39 | 2 | 0 |
Anorectal Diseases [description not available] | 0 | 3.84 | 4 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 3.84 | 4 | 0 |
Carcinoma, Embryonal A highly malignant, primitive form of carcinoma, probably of germinal cell or teratomatous derivation, usually arising in a gonad and rarely in other sites. It is rare in the female ovary, but in the male it accounts for 20% of all testicular tumors. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, p1595) | 0 | 3.61 | 9 | 0 |
Seminoma A radiosensitive, malignant neoplasm of the testis, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. There are three variants: classical (typical), the most common type; anaplastic; and spermatocytic. The classical seminoma is composed of fairly well differentiated sheets or cords of uniform polygonal or round cells (seminoma cells), each cell having abundant clear cytoplasm, distinct cell membranes, a centrally placed round nucleus, and one or more nucleoli. In the female, a grossly and histologically identical neoplasm, known as dysgerminoma, occurs. (Dorland, 27th ed) | 0 | 3.8 | 11 | 0 |
Molluscum Contagiosum A common, benign, usually self-limited viral infection of the skin and occasionally the conjunctivae by a poxvirus (MOLLUSCUM CONTAGIOSUM VIRUS). (Dorland, 27th ed) | 0 | 3.48 | 8 | 0 |
Smooth Muscle Tumor A tumor composed of smooth muscle tissue, as opposed to leiomyoma, a tumor derived from smooth muscle. | 0 | 2.43 | 2 | 0 |
Carcinoma, Skin Appendage A malignant tumor of the skin appendages, which include the hair, nails, sebaceous glands, sweat glands, and the mammary glands. (From Dorland, 27th ed) | 0 | 3.26 | 6 | 0 |
FMR1-Related Primary Ovarian Insufficiency [description not available] | 0 | 2.05 | 1 | 0 |
Primary Ovarian Insufficiency Cessation of ovarian function after MENARCHE but before the age of 40, without or with OVARIAN FOLLICLE depletion. It is characterized by the presence of OLIGOMENORRHEA or AMENORRHEA, elevated GONADOTROPINS, and low ESTRADIOL levels. It is a state of female HYPERGONADOTROPIC HYPOGONADISM. Etiologies include genetic defects, autoimmune processes, chemotherapy, radiation, and infections. The most commonly known genetic cause is the expansion of a CGG repeat to 55 to 199 copies in the 5' untranslated region in the X-linked FMR1 gene. | 0 | 2.05 | 1 | 0 |
Neoplasms, Nerve Sheath [description not available] | 0 | 5.33 | 13 | 0 |
Nerve Sheath Neoplasms Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category. | 0 | 5.33 | 13 | 0 |
Epidermodysplasia Verruciformis An autosomal recessive trait with impaired cell-mediated immunity. About 15 human papillomaviruses are implicated in associated infection, four of which lead to skin neoplasms. The disease begins in childhood with red papules and later spreads over the body as gray or yellow scales. | 0 | 2.05 | 1 | 0 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 2.43 | 2 | 0 |
Impaired Glucose Tolerance [description not available] | 0 | 2.05 | 1 | 0 |
Glucose Intolerance A pathological state in which BLOOD GLUCOSE level is less than approximately 140 mg/100 ml of PLASMA at fasting, and above approximately 200 mg/100 ml plasma at 30-, 60-, or 90-minute during a GLUCOSE TOLERANCE TEST. This condition is seen frequently in DIABETES MELLITUS, but also occurs with other diseases and MALNUTRITION. | 0 | 2.05 | 1 | 0 |
Brain Stem Neoplasms, Primary [description not available] | 0 | 2.05 | 1 | 0 |
Brain Stem Neoplasms Benign and malignant intra-axial tumors of the MESENCEPHALON; PONS; or MEDULLA OBLONGATA of the BRAIN STEM. Primary and metastatic neoplasms may occur in this location. Clinical features include ATAXIA, cranial neuropathies (see CRANIAL NERVE DISEASES), NAUSEA, hemiparesis (see HEMIPLEGIA), and quadriparesis. Primary brain stem neoplasms are more frequent in children. Histologic subtypes include GLIOMA; HEMANGIOBLASTOMA; GANGLIOGLIOMA; and EPENDYMOMA. | 0 | 2.05 | 1 | 0 |
Choroid Neovascularization [description not available] | 0 | 4.95 | 14 | 0 |
Hemolysis, Elevated Liver Enzymes, Lowered Platelets [description not available] | 0 | 2.05 | 1 | 0 |
Gestational Hypertension [description not available] | 0 | 2.05 | 1 | 0 |
HELLP Syndrome A syndrome of HEMOLYSIS, elevated liver ENZYMES, and low blood platelets count (THROMBOCYTOPENIA). HELLP syndrome is observed in pregnant women with PRE-ECLAMPSIA or ECLAMPSIA who also exhibit LIVER damage and abnormalities in BLOOD COAGULATION. | 0 | 2.05 | 1 | 0 |
Hypertension, Pregnancy-Induced A condition in pregnant women with elevated systolic ( | 0 | 2.05 | 1 | 0 |
Syringoma A benign tumor of the sweat glands which is usually multiple and results from malformation of sweat ducts. It is uncommon and more common in females than in males. It is most likely to appear at adolescence, and further lesions may develop during adult life. It does not appear to be hereditary. (Rook et al., Textbook of Dermatology, 4th ed, pp2407-8) | 0 | 5.06 | 16 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 3.58 | 9 | 0 |
Break-Bone Fever [description not available] | 0 | 2.05 | 1 | 0 |
Alpha Virus Infections [description not available] | 0 | 2.05 | 1 | 0 |
Dengue An acute febrile disease transmitted by the bite of AEDES mosquitoes infected with DENGUE VIRUS. It is self-limiting and characterized by fever, myalgia, headache, and rash. SEVERE DENGUE is a more virulent form of dengue. | 0 | 2.05 | 1 | 0 |
Fasciolopsiasis [description not available] | 0 | 2.05 | 1 | 0 |
Root Resorption Resorption in which cementum or dentin is lost from the root of a tooth owing to cementoclastic or osteoclastic activity in conditions such as trauma of occlusion or neoplasms. (Dorland, 27th ed) | 0 | 3.09 | 5 | 0 |
Dentin Dysplasia An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed) | 0 | 2.96 | 1 | 0 |
Gingival Pocket An abnormal extension of a gingival sulcus not accompanied by the apical migration of the epithelial attachment. | 0 | 11.39 | 24 | 14 |
Erythroplasia A condition of the mucous membrane characterized by erythematous papular lesions. | 0 | 5.06 | 6 | 0 |
Lymphoma of Mucosa-Associated Lymphoid Tissue [description not available] | 0 | 4.63 | 10 | 0 |
Adenitis, Salivary Gland [description not available] | 0 | 4.51 | 9 | 0 |
Parotid Diseases Diseases involving the PAROTID GLAND. | 0 | 4.64 | 6 | 0 |
AIDS-Related Opportunistic Infections Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus. | 0 | 3.33 | 2 | 0 |
Lymphoma, B-Cell, Marginal Zone Extranodal lymphoma of lymphoid tissue associated with mucosa that is in contact with exogenous antigens. Many of the sites of these lymphomas, such as the stomach, salivary gland, and thyroid, are normally devoid of lymphoid tissue. They acquire mucosa-associated lymphoid tissue (MALT) type as a result of an immunologically mediated disorder. | 0 | 4.63 | 10 | 0 |
Envenomation, Snakebite [description not available] | 0 | 2.05 | 1 | 0 |
Abnormalities, Autosome [description not available] | 0 | 8.7 | 65 | 0 |
Mastitis INFLAMMATION of the BREAST, or MAMMARY GLAND. | 0 | 3.23 | 6 | 0 |
Tonsillitis Inflammation of the tonsils, especially the PALATINE TONSILS but the ADENOIDS (pharyngeal tonsils) and lingual tonsils may also be involved. Tonsillitis usually is caused by bacterial infection. Tonsillitis may be acute, chronic, or recurrent. | 0 | 4.16 | 6 | 0 |
Leukoma [description not available] | 0 | 5.76 | 13 | 0 |
Corneal Opacity Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque. | 0 | 5.76 | 13 | 0 |
Disease, Pulmonary [description not available] | 0 | 6.29 | 36 | 0 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 6.29 | 36 | 0 |
Adenomatous Polyposis Coli, Familial [description not available] | 0 | 3.83 | 4 | 0 |
Adenomatous Polyposis Coli A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood. | 0 | 3.83 | 4 | 0 |
Complex Regional Pain Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Complex Regional Pain Syndromes Conditions characterized by pain involving an extremity or other body region, HYPERESTHESIA, and localized autonomic dysfunction following injury to soft tissue or nerve. The pain is usually associated with ERYTHEMA; SKIN TEMPERATURE changes, abnormal sudomotor activity (i.e., changes in sweating due to altered sympathetic innervation) or edema. The degree of pain and other manifestations is out of proportion to that expected from the inciting event. Two subtypes of this condition have been described: type I; (REFLEX SYMPATHETIC DYSTROPHY) and type II; (CAUSALGIA). (From Pain 1995 Oct;63(1):127-33) | 0 | 2.05 | 1 | 0 |
Sarcoma, Small Cell A sarcoma characterized by the presence of small cells, cells measuring 9-14 micrometers with a faint or indistinct rim of cytoplasm and an oval-to-elongated nucleus with relatively dense chromatin. (From Segen, Dictionary of Modern Medicine, 1992) | 0 | 3.26 | 6 | 0 |
Palatal Neoplasms Tumors or cancer of the PALATE, including those of the hard palate, soft palate and UVULA. | 0 | 5.67 | 31 | 0 |
Injuries, Eye [description not available] | 0 | 5.69 | 7 | 0 |
Absent Iris [description not available] | 0 | 2.93 | 4 | 0 |
Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | 0 | 5.69 | 7 | 0 |
Aniridia A congenital abnormality in which there is only a rudimentary iris. This is due to the failure of the optic cup to grow. Aniridia also occurs in a hereditary form, usually autosomal dominant. | 0 | 2.93 | 4 | 0 |
Disc, Herniated [description not available] | 0 | 4.48 | 5 | 0 |
Intervertebral Disc Displacement An INTERVERTEBRAL DISC in which the NUCLEUS PULPOSUS has protruded through surrounding ANNULUS FIBROSUS. This occurs most frequently in the lower lumbar region. | 0 | 4.48 | 5 | 0 |
Pterygium An abnormal triangular fold of membrane in the interpalpebral fissure, extending from the conjunctiva to the cornea, being immovably united to the cornea at its apex, firmly attached to the sclera throughout its middle portion, and merged with the conjunctiva at its base. (Dorland, 27th ed) | 0 | 3.27 | 6 | 0 |
Candida Infection [description not available] | 0 | 3.07 | 5 | 0 |
Candidiasis Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ed) | 0 | 3.07 | 5 | 0 |
Hemoptysis Expectoration or spitting of blood originating from any part of the RESPIRATORY TRACT, usually from hemorrhage in the lung parenchyma (PULMONARY ALVEOLI) and the BRONCHIAL ARTERIES. | 0 | 2.43 | 2 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 7.72 | 27 | 1 |
Pulmonary Fibrosis A process in which normal lung tissues are progressively replaced by FIBROBLASTS and COLLAGEN causing an irreversible loss of the ability to transfer oxygen into the bloodstream via PULMONARY ALVEOLI. Patients show progressive DYSPNEA finally resulting in death. | 0 | 7.72 | 27 | 1 |
Dysesthesia [description not available] | 0 | 2.05 | 1 | 0 |
Conus Medullaris Syndrome [description not available] | 0 | 3.38 | 2 | 0 |
Central Nervous System Cysts Congenital or acquired cysts of the brain, spinal cord, or meninges which may remain stable in size or undergo progressive enlargement. | 0 | 3.64 | 9 | 0 |
Adenocarcinoma, Alveolar [description not available] | 0 | 5.63 | 18 | 0 |
Adenocarcinoma, Bronchiolo-Alveolar A carcinoma derived from epithelium of terminal bronchioles, in which the neoplastic tissue extends along the alveolar walls and grows in small masses within the alveoli. Involvement may be uniformly diffuse and massive, or nodular, or lobular. The neoplastic cells are cuboidal or columnar and form papillary structures. Mucin may be demonstrated in some of the cells and in the material in the alveoli, which also includes denuded cells. Metastases in regional lymph nodes, and in even more distant sites, are known to occur, but are infrequent. (From Stedman, 25th ed) | 0 | 5.63 | 18 | 0 |
Proliferative Vitreoretinopathy [description not available] | 0 | 4.41 | 21 | 0 |
Vitreoretinopathy, Proliferative Vitreoretinal membrane shrinkage or contraction secondary to the proliferation of primarily retinal pigment epithelial cells and glial cells, particularly fibrous astrocytes, followed by membrane formation. The formation of fibrillar collagen and cellular proliferation appear to be the basis for the contractile properties of the epiretinal and vitreous membranes. | 0 | 4.41 | 21 | 0 |
Infectious Skin Diseases [description not available] | 0 | 3.66 | 10 | 0 |
Skin Diseases, Infectious Skin diseases caused by bacteria, fungi, parasites, or viruses. | 0 | 3.66 | 10 | 0 |
Infectious Myelitis [description not available] | 0 | 2.05 | 1 | 0 |
Hepatoblastoma A malignant neoplasm occurring in young children, primarily in the liver, composed of tissue resembling embryonal or fetal hepatic epithelium, or mixed epithelial and mesenchymal tissues. (Stedman, 25th ed) | 0 | 5.26 | 12 | 0 |
Bile Reflux Retrograde bile flow. Reflux of bile can be from the duodenum to the stomach (DUODENOGASTRIC REFLUX); to the esophagus (GASTROESOPHAGEAL REFLUX); or to the PANCREAS. | 0 | 2.05 | 1 | 0 |
Autoimmune Diabetes [description not available] | 0 | 4.62 | 10 | 0 |
Diabetes Mellitus, Type 1 A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence. | 0 | 4.62 | 10 | 0 |
Benign Mucosal Pemphigoid [description not available] | 0 | 3.25 | 6 | 0 |
Pemphigoid, Benign Mucous Membrane A chronic blistering disease with predilection for mucous membranes and less frequently the skin, and with a tendency to scarring. It is sometimes called ocular pemphigoid because of conjunctival mucous membrane involvement. | 0 | 3.25 | 6 | 0 |
Foreign-Body Reaction Chronic inflammation and granuloma formation around irritating foreign bodies. | 0 | 4.41 | 8 | 0 |
Fat Necrosis A condition in which the death of adipose tissue results in neutral fats being split into fatty acids and glycerol. | 0 | 2.42 | 2 | 0 |
Netherton Disease [description not available] | 0 | 2.05 | 1 | 0 |
Netherton Syndrome Rare autosomal recessive disease with variable expressions. Clinical features of the disease include variable ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; bamboo hair (trichorrhexis invaginata); and ATOPIC DERMATITIS. The disease is caused by mutations in the SPINK5 gene. | 0 | 2.05 | 1 | 0 |
Benign Cranial Nerve Neoplasms [description not available] | 0 | 2.69 | 3 | 0 |
Male Genital Neoplasms [description not available] | 0 | 5.41 | 10 | 0 |
Genital Neoplasms, Male Tumor or cancer of the MALE GENITALIA. | 0 | 5.41 | 10 | 0 |
Alcoholic Liver Diseases [description not available] | 0 | 4.98 | 15 | 0 |
Liver Diseases, Alcoholic Liver diseases associated with ALCOHOLISM. It usually refers to the coexistence of two or more subentities, i.e., ALCOHOLIC FATTY LIVER; ALCOHOLIC HEPATITIS; and ALCOHOLIC CIRRHOSIS. | 0 | 4.98 | 15 | 0 |
Anaplasia Loss of structural differentiation and useful function of neoplastic cells. | 0 | 4.28 | 7 | 0 |
Genome Instability [description not available] | 0 | 2.74 | 3 | 0 |
Corneal Angiogenesis [description not available] | 0 | 2.94 | 4 | 0 |
Corneal Neovascularization New blood vessels originating from the corneal blood vessels and extending from the limbus into the adjacent CORNEAL STROMA. Neovascularization in the superficial and/or deep corneal stroma is a sequel to numerous inflammatory diseases of the ocular anterior segment, such as TRACHOMA, viral interstitial KERATITIS, microbial KERATOCONJUNCTIVITIS, and the immune response elicited by CORNEAL TRANSPLANTATION. | 0 | 2.94 | 4 | 0 |
Acoustic Neurinoma, Bilateral [description not available] | 0 | 3.36 | 2 | 0 |
Neurofibromatosis 2 An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life. | 0 | 3.36 | 2 | 0 |
Corneal Edema An excessive amount of fluid in the cornea due to damage of the epithelium or endothelium causing decreased visual acuity. | 0 | 2.46 | 2 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 4.6 | 10 | 0 |
Tooth Diseases Diseases involving the TEETH. | 0 | 2.97 | 1 | 0 |
Feuerstein-Mims Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Choroid Plexus Papilloma [description not available] | 0 | 2.72 | 3 | 0 |
Bright Disease A historical classification which is no longer used. It described acute glomerulonephritis, acute nephritic syndrome, or acute nephritis. Named for Richard Bright. | 0 | 3.94 | 13 | 0 |
Glomerulonephritis Inflammation of the renal glomeruli (KIDNEY GLOMERULUS) that can be classified by the type of glomerular injuries including antibody deposition, complement activation, cellular proliferation, and glomerulosclerosis. These structural and functional abnormalities usually lead to HEMATURIA; PROTEINURIA; HYPERTENSION; and RENAL INSUFFICIENCY. | 0 | 3.94 | 13 | 0 |
Acrospiroma A rare cutaneous tumor of apocrine or eccrine SWEAT GLAND origin. It is most commonly found on the extremities and is usually benign. It appears as a solitary nodule or cyst and may be solid or produce a watery discharge. It is related to POROMA except in acrospiroma it does not involve the epidermis. There is no indication that heredity or external agents cause these tumors. | 0 | 5.78 | 21 | 0 |
Injuries, Soft Tissue [description not available] | 0 | 2.06 | 1 | 0 |
Hand Injuries General or unspecified injuries to the hand. | 0 | 2.06 | 1 | 0 |
Appendiceal Cancer [description not available] | 0 | 3.94 | 13 | 0 |
Appendiceal Neoplasms Tumors or cancer of the APPENDIX. | 0 | 3.94 | 13 | 0 |
Papilloma, Inverted A mucosal tumor of the urinary bladder or nasal cavity in which proliferating epithelium is invaginated beneath the surface and is more smoothly rounded than in other papillomas. (Stedman, 25th ed) | 0 | 3.38 | 7 | 0 |
Epulides, Giant Cell [description not available] | 0 | 4.17 | 6 | 0 |
Cherubism A fibro-osseous hereditary disease of the jaws. The swollen jaws and raised eyes give a cherubic appearance; multiple radiolucencies are evident upon radiographic examination. | 0 | 2.04 | 1 | 0 |
Granuloma, Giant Cell A non-neoplastic inflammatory lesion, usually of the jaw or gingiva, containing large, multinucleated cells. It includes reparative giant cell granuloma. Peripheral giant cell granuloma refers to the gingiva (giant cell epulis); central refers to the jaw. | 0 | 4.17 | 6 | 0 |
Bare Lymphocyte Syndrome [description not available] | 0 | 3.1 | 5 | 0 |
Severe Combined Immunodeficiency Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID). | 0 | 3.1 | 5 | 0 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 4.62 | 6 | 0 |
Neurofibromatosis 1 An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS). | 0 | 4.62 | 6 | 0 |
Sertoli Cell Tumor Gonadal neoplasm composed entirely of SERTOLI CELLS or may have a component of GRANULOSA CELLS. Some of the Sertoli cell tumors produce ESTROGEN or ANDROGENS, but seldom in sufficient quantity to cause clinical symptoms such as FEMINIZATION or masculinization (VIRILISM). | 0 | 4.92 | 14 | 0 |
Cystadenocarcinoma, Papillary An adenocarcinoma in which the tumor elements are arranged as finger-like processes or as a solid spherical nodule projecting from an epithelial surface. | 0 | 4.72 | 11 | 0 |
Maxillary Diseases Diseases involving the MAXILLA. | 0 | 6.82 | 45 | 0 |
Nonodontogenic Cysts Cysts formed from epithelial inclusions in the lines of fusion of the embryonic processes which form the jaws. They include nasopalatine or incisive canal cyst, incisive papilla cyst, globulomaxillary cyst, median palatal cyst, median alveolar cyst, median mandibular cyst, and nasoalveolar cyst. | 0 | 4.96 | 15 | 0 |
Licheniform Eruptions [description not available] | 0 | 3.11 | 5 | 0 |
Corneal Endothelial Cell Damage [description not available] | 0 | 2.05 | 1 | 0 |
Eye Infections, Fungal Infection by a variety of fungi, usually through four possible mechanisms: superficial infection producing conjunctivitis, keratitis, or lacrimal obstruction; extension of infection from neighboring structures - skin, paranasal sinuses, nasopharynx; direct introduction during surgery or accidental penetrating trauma; or via the blood or lymphatic routes in patients with underlying mycoses. | 0 | 2.05 | 1 | 0 |
Bladder Exstrophy A birth defect in which the URINARY BLADDER is malformed and exposed, inside out, and protruded through the ABDOMINAL WALL. It is caused by closure defects involving the top front surface of the bladder, as well as the lower abdominal wall; SKIN; MUSCLES; and the pubic bone. | 0 | 2.38 | 2 | 0 |
Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | 0 | 2.06 | 1 | 0 |
Congenital Ichthyosiform Erythroderma [description not available] | 0 | 3.59 | 9 | 0 |
Neovascularization, Optic Disc [description not available] | 0 | 3.1 | 5 | 0 |
Retinal Neovascularization Formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina. | 0 | 3.1 | 5 | 0 |
Ichthyosis Simplex [description not available] | 0 | 4.01 | 5 | 0 |
Multiple Hemangioblastomas [description not available] | 0 | 4.18 | 6 | 0 |
Erythrocytosis [description not available] | 0 | 2.05 | 1 | 0 |
Low Back Ache [description not available] | 0 | 2.05 | 1 | 0 |
Low Back Pain Acute or chronic pain in the lumbar or sacral regions, which may be associated with musculo-ligamentous SPRAINS AND STRAINS; INTERVERTEBRAL DISK DISPLACEMENT; and other conditions. | 0 | 2.05 | 1 | 0 |
Hemangioblastoma A benign tumor of the nervous system that may occur sporadically or in association with VON HIPPEL-LINDAU DISEASE. It accounts for approximately 2% of intracranial tumors, arising most frequently in the cerebellar hemispheres and vermis. Histologically, the tumors are composed of multiple capillary and sinusoidal channels lined with endothelial cells and clusters of lipid-laden pseudoxanthoma cells. Usually solitary, these tumors can be multiple and may also occur in the brain stem, spinal cord, retina, and supratentorial compartment. Cerebellar hemangioblastomas usually present in the third decade with INTRACRANIAL HYPERTENSION, and ataxia. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2071-2) | 0 | 4.18 | 6 | 0 |
Segond Fracture [description not available] | 0 | 2.05 | 1 | 0 |
Tibial Fractures Fractures of the TIBIA. | 0 | 2.05 | 1 | 0 |
Gammapathy, Monoclonal [description not available] | 0 | 2.05 | 1 | 0 |
Paraproteinemias A group of related diseases characterized by an unbalanced or disproportionate proliferation of immunoglobulin-producing cells, usually from a single clone. These cells frequently secrete a structurally homogeneous immunoglobulin (M-component) and/or an abnormal immunoglobulin. | 0 | 2.05 | 1 | 0 |
Isochromosomes Metacentric chromosomes produced during MEIOSIS or MITOSIS when the CENTROMERE splits transversely instead of longitudinally. The chromosomes produced by this abnormal division are one chromosome having the two long arms of the original chromosome, but no short arms, and the other chromosome consisting of the two short arms and no long arms. Each of these isochromosomes constitutes a simultaneous duplication and deletion. | 0 | 2.06 | 1 | 0 |
Chromosomal Duplication [description not available] | 0 | 2.06 | 1 | 0 |
Neoplasms, Vascular [description not available] | 0 | 3.39 | 7 | 0 |
Chondroblastoma A usually benign tumor composed of cells which arise from chondroblasts or their precursors and which tend to differentiate into cartilage cells. It occurs primarily in the epiphyses of adolescents. It is relatively rare and represents less than 2% of all primary bone tumors. The peak incidence is in the second decade of life; it is about twice as common in males as in females. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1846) | 0 | 3.11 | 5 | 0 |
Abdominal Hernia [description not available] | 0 | 2.05 | 1 | 0 |
Anhidrosis [description not available] | 0 | 2.06 | 1 | 0 |
Hives [description not available] | 0 | 2.38 | 2 | 0 |
Urticaria A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress. | 0 | 2.38 | 2 | 0 |
Breast Cancer, Male [description not available] | 0 | 5.97 | 14 | 0 |
Breast Neoplasms, Male Any neoplasms of the male breast. These occur infrequently in males in developed countries, the incidence being about 1% of that in females. | 0 | 5.97 | 14 | 0 |
Carcinoma, Basosquamous A skin carcinoma that histologically exhibits both basal and squamous elements. (From Dorland, 27th ed) | 0 | 4.14 | 16 | 0 |
Bile Duct Diseases Diseases in any part of the ductal system of the BILIARY TRACT from the smallest BILE CANALICULI to the largest COMMON BILE DUCT. | 0 | 4.16 | 6 | 0 |
Krukenberg Carcinoma [description not available] | 0 | 2.44 | 2 | 0 |
Cancer of Cecum [description not available] | 0 | 3.24 | 6 | 0 |
Hematologic Malignancies [description not available] | 0 | 2.43 | 2 | 0 |
Hematologic Neoplasms Neoplasms located in the blood and blood-forming tissue (the bone marrow and lymphatic tissue). The commonest forms are the various types of LEUKEMIA, of LYMPHOMA, and of the progressive, life-threatening forms of the MYELODYSPLASTIC SYNDROMES. | 0 | 2.43 | 2 | 0 |
Polyploid [description not available] | 0 | 4.01 | 14 | 0 |
Familial Nonmedullary Thyroid Cancer [description not available] | 0 | 2.47 | 2 | 0 |
Autoimmune Chronic Hepatitis [description not available] | 0 | 3.4 | 7 | 0 |
Hepatitis, Autoimmune A chronic self-perpetuating hepatocellular INFLAMMATION of unknown cause, usually with HYPERGAMMAGLOBULINEMIA and serum AUTOANTIBODIES. | 0 | 3.4 | 7 | 0 |
Autism [description not available] | 0 | 2.06 | 1 | 0 |
Autistic Disorder A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V) | 0 | 2.06 | 1 | 0 |
Orbital Neoplasms Neoplasms of the bony orbit and contents except the eyeball. | 0 | 3.87 | 12 | 0 |
Harelip [description not available] | 0 | 3.08 | 5 | 0 |
Cleft Palate, Isolated [description not available] | 0 | 3.39 | 7 | 0 |
Cleft Lip Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region. | 0 | 3.08 | 5 | 0 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 3.39 | 7 | 0 |
Diverticulum, Meckel [description not available] | 0 | 2.05 | 1 | 0 |
Angioimmunoblastic Lymphadenopathy [description not available] | 0 | 2.06 | 1 | 0 |
Brill-Symmers Disease [description not available] | 0 | 2.45 | 2 | 0 |
T-Cell Lymphoma [description not available] | 0 | 2.42 | 2 | 0 |
Lymphoma, T Cell, Peripheral [description not available] | 0 | 2.06 | 1 | 0 |
Immunoblastic Lymphadenopathy A disorder characterized by proliferation of arborizing small vessels, prominent immunoblastic proliferations and amorphous acidophilic interstitial material. Clinical manifestations include fever, sweats, weight loss, generalized lymphadenopathy and frequently hepatosplenomegaly. | 0 | 2.06 | 1 | 0 |
Lymphoma, Follicular Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES. | 0 | 2.45 | 2 | 0 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 2.42 | 2 | 0 |
Lymphoma, T-Cell, Peripheral A group of malignant lymphomas thought to derive from peripheral T-lymphocytes in lymph nodes and other nonlymphoid sites. They include a broad spectrum of lymphocyte morphology, but in all instances express T-cell markers admixed with epithelioid histiocytes, plasma cells, and eosinophils. Although markedly similar to large-cell immunoblastic lymphoma (LYMPHOMA, LARGE-CELL, IMMUNOBLASTIC), this group's unique features warrant separate treatment. | 0 | 2.06 | 1 | 0 |
Endothelioma, Vascular [description not available] | 0 | 3.1 | 5 | 0 |
Hemangioendothelioma A neoplasm derived from blood vessels, characterized by numerous prominent endothelial cells that occur singly, in aggregates, and as the lining of congeries of vascular tubes or channels. Hemangioendotheliomas are relatively rare and are of intermediate malignancy (between benign hemangiomas and conventional angiosarcomas). They affect men and women about equally and rarely develop in childhood. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1866) | 0 | 3.1 | 5 | 0 |
Glomerulonephritis, Lupus [description not available] | 0 | 2.72 | 3 | 0 |
Anti-GBM Disease [description not available] | 0 | 2.44 | 2 | 0 |
Lupus Nephritis Glomerulonephritis associated with autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Lupus nephritis is histologically classified into 6 classes: class I - normal glomeruli, class II - pure mesangial alterations, class III - focal segmental glomerulonephritis, class IV - diffuse glomerulonephritis, class V - diffuse membranous glomerulonephritis, and class VI - advanced sclerosing glomerulonephritis (The World Health Organization classification 1982). | 0 | 2.72 | 3 | 0 |
Anti-Glomerular Basement Membrane Disease An autoimmune disease of the KIDNEY and the LUNG. It is characterized by the presence of circulating autoantibodies targeting the epitopes in the non-collagenous domains of COLLAGEN TYPE IV in the basement membranes of kidney glomeruli (KIDNEY GLOMERULUS) and lung alveoli (PULMONARY ALVEOLI), and the subsequent destruction of these basement membranes. Clinical features include pulmonary alveolar hemorrhage and glomerulonephritis. | 0 | 2.44 | 2 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 2.94 | 4 | 0 |
Gestational Trophoblastic Neoplasia Gestational Trophoblastic diseases that are malignant. It does not include HYDATIDIFORM MOLE. However, there is a minority of authors that consider the term gestational trophoblastic neoplasia synonymous with gestational trophoblastic disease. | 0 | 2.06 | 1 | 0 |
Gestational Trophoblastic Disease A group of diseases arising from pregnancy that are commonly associated with hyperplasia of trophoblasts (TROPHOBLAST) and markedly elevated human CHORIONIC GONADOTROPIN. They include HYDATIDIFORM MOLE, invasive mole (HYDATIDIFORM MOLE, INVASIVE), placental-site trophoblastic tumor (TROPHOBLASTIC TUMOR, PLACENTAL SITE), and CHORIOCARCINOMA. These neoplasms have varying propensities for invasion and spread. | 0 | 2.06 | 1 | 0 |
Embolism, Pulmonary [description not available] | 0 | 3.08 | 5 | 0 |
Linitis Plastica A condition where the stomach wall becomes thickened, rubbery and loses its ability to distend. The stomach assumes a leather bottle shape. It is most often seen in adenocarcinoma of the stomach. The term is often used synonymously with diffuse adenocarcinoma of the stomach. | 0 | 2.69 | 3 | 0 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 3.08 | 5 | 0 |
Central Nervous System Disease [description not available] | 0 | 4.47 | 5 | 0 |
Central Nervous System Diseases Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord. | 0 | 4.47 | 5 | 0 |
Fibro-Odontoma [description not available] | 0 | 3.87 | 12 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 4.01 | 5 | 0 |
Conductive Hearing Loss [description not available] | 0 | 2.71 | 3 | 0 |
Pulsatile Tinnitus [description not available] | 0 | 2.07 | 1 | 0 |
Tinnitus A nonspecific symptom of hearing disorder characterized by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear. Objective tinnitus refers to noises generated from within the ear or adjacent structures that can be heard by other individuals. The term subjective tinnitus is used when the sound is audible only to the affected individual. Tinnitus may occur as a manifestation of COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; and other conditions. | 0 | 2.07 | 1 | 0 |
Fever of Unknown Origin Fever in which the etiology cannot be ascertained. | 0 | 2.06 | 1 | 0 |
Aphthae [description not available] | 0 | 3.8 | 4 | 0 |
Stomatitis, Aphthous A recurrent disease of the oral mucosa of unknown etiology. It is characterized by small white ulcerative lesions, single or multiple, round or oval. Two to eight crops of lesions occur per year, lasting for 7 to 14 days and then heal without scarring. (From Jablonski's Dictionary of Dentistry, 1992, p742) | 0 | 3.8 | 4 | 0 |
alpha 1-Antitrypsin Deficiency Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS. | 0 | 4.17 | 6 | 0 |
Eccrine Porocarcinoma A rare malignant neoplasm of the sweat glands. It most often develops as a form of degenerative progression from a benign ECCRINE POROMA. | 0 | 2.47 | 2 | 0 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 6.95 | 9 | 1 |
Gastroenteritis INFLAMMATION of any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. Causes of gastroenteritis are many including genetic, infection, HYPERSENSITIVITY, drug effects, and CANCER. | 0 | 2.06 | 1 | 0 |
Rotavirus Infections Infection with any of the rotaviruses. Specific infections include human infantile diarrhea, neonatal calf diarrhea, and epidemic diarrhea of infant mice. | 0 | 2.42 | 2 | 0 |
Ventral Hernia [description not available] | 0 | 2.06 | 1 | 0 |
Hernia, Ventral A hernia caused by weakness of the anterior ABDOMINAL WALL due to midline defects, previous incisions, or increased intra-abdominal pressure. Ventral hernias include UMBILICAL HERNIA, incisional, epigastric, and spigelian hernias. | 0 | 2.06 | 1 | 0 |
Hydatid Cyst of Morgagni [description not available] | 0 | 2.98 | 1 | 0 |
Day Blindness [description not available] | 0 | 3.64 | 3 | 0 |
Allergic Bronchopulmonary Mycosis [description not available] | 0 | 2.06 | 1 | 0 |
Adenitis [description not available] | 0 | 2.06 | 1 | 0 |
Neoplasms, Otorhinolaryngologic [description not available] | 0 | 3.38 | 7 | 0 |
Myosarcoma A general term for a malignant neoplasm derived from muscular tissue. (Stedman, 25th ed) | 0 | 2.06 | 1 | 0 |
Bacterial Disease [description not available] | 0 | 5.18 | 8 | 0 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 5.18 | 8 | 0 |
Atypical Mycobacterial Infection, Disseminated [description not available] | 0 | 2.06 | 1 | 0 |
BOOP [description not available] | 0 | 2.43 | 2 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 6.65 | 29 | 0 |
Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. | 0 | 6.65 | 29 | 0 |
Burning Mouth Syndrome A group of painful oral symptoms associated with a burning or similar sensation. There is usually a significant organic component with a degree of functional overlay; it is not limited to the psychophysiologic group of disorders. | 0 | 2.07 | 1 | 0 |
Earache Pain in the ear. | 0 | 2.06 | 1 | 0 |
Central Hypothyroidism [description not available] | 0 | 2.89 | 4 | 0 |
Hypothyroidism A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction. | 0 | 2.89 | 4 | 0 |
Cardiac Remodeling, Ventricular [description not available] | 0 | 2.06 | 1 | 0 |
Cardiovascular Stroke [description not available] | 0 | 2.06 | 1 | 0 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 2.06 | 1 | 0 |
Cranial Nerve II Injuries [description not available] | 0 | 2.07 | 1 | 0 |
Muscle Disorders [description not available] | 0 | 4.29 | 4 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 4.29 | 4 | 0 |
Experimental Hepatoma [description not available] | 0 | 6.64 | 52 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 2.45 | 2 | 0 |
Nerve Degeneration Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways. | 0 | 2.93 | 4 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 2.45 | 2 | 0 |
Glaucoma An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed) | 0 | 2.69 | 3 | 0 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 2.41 | 2 | 0 |
Abdominal Cryptorchidism [description not available] | 0 | 2.7 | 3 | 0 |
Hypotrichosis Presence of less than the normal amount of hair. (Dorland, 27th ed) | 0 | 3.85 | 4 | 0 |
Uveitis, Anterior Inflammation of the anterior uvea comprising the iris, angle structures, and the ciliary body. Manifestations of this disorder include ciliary injection, exudation into the anterior chamber, iris changes, and adhesions between the iris and lens (posterior synechiae). Intraocular pressure may be increased or reduced. | 0 | 2.07 | 1 | 0 |
Hemangioma, Sclerosing, Pulmonary [description not available] | 0 | 2.97 | 4 | 0 |
Muscle Contraction A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments. | 0 | 2.89 | 4 | 0 |
Leishmaniasis, American [description not available] | 0 | 2.06 | 1 | 0 |
Leishmaniasis, Cutaneous An endemic disease that is characterized by the development of single or multiple localized lesions on exposed areas of skin that typically ulcerate. The disease has been divided into Old and New World forms. Old World leishmaniasis is separated into three distinct types according to epidemiology and clinical manifestations and is caused by species of the L. tropica and L. aethiopica complexes as well as by species of the L. major genus. New World leishmaniasis, also called American leishmaniasis, occurs in South and Central America and is caused by species of the L. mexicana or L. braziliensis complexes. | 0 | 2.06 | 1 | 0 |
Nearsightedness [description not available] | 0 | 2.48 | 2 | 0 |
Myopia A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness. | 0 | 2.48 | 2 | 0 |
Respiratory Tract Neoplasms New abnormal growth of tissue in the RESPIRATORY SYSTEM. | 0 | 4.76 | 7 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 4 | 5 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 4 | 5 | 0 |
Splenic Diseases Diseases involving the SPLEEN. | 0 | 4.17 | 6 | 0 |
Cancer of Intestines [description not available] | 0 | 5.69 | 19 | 0 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 5.69 | 19 | 0 |
Corneal Dystrophy, Juvenile Epithelial of Meesmann An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder. | 0 | 2.06 | 1 | 0 |
Mucopolysaccharidosis [description not available] | 0 | 4.26 | 4 | 1 |
Mucopolysaccharidoses Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. | 0 | 4.26 | 4 | 1 |
Cockayne-Touraine Disease [description not available] | 0 | 4.02 | 5 | 0 |
Epidermolysis Bullosa Dystrophica Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS. | 0 | 4.02 | 5 | 0 |
Hemothorax Hemorrhage within the pleural cavity. | 0 | 2.45 | 2 | 0 |
Mixed Tumor, Mullerian A tumor, basically a carcinoma with a single sarcoma such as leiomyosarcoma or angiosarcoma or multiple sarcomas of uterine origin. The role of estrogen has been postulated as a possible etiological factor in this tumor. (Holland et al., Cancer Medicine, 3d ed, p1703) | 0 | 5 | 9 | 0 |
Sublingual Gland Neoplasms Neoplasms of the sublingual glands. | 0 | 2.42 | 2 | 0 |
Scrotal Hydrocele [description not available] | 0 | 2.42 | 2 | 0 |
Benign Monoclonal Gammopathies [description not available] | 0 | 2.99 | 1 | 0 |
Cancer of the Tonsil [description not available] | 0 | 4.15 | 6 | 0 |
Tonsillar Neoplasms Tumors or cancer of the PALATINE TONSIL. | 0 | 4.15 | 6 | 0 |
Koch's Disease [description not available] | 0 | 2.43 | 2 | 0 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 2.43 | 2 | 0 |
Lymphocytopenia [description not available] | 0 | 3.46 | 1 | 1 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 3.46 | 1 | 1 |
Carcinomatous Meningitis [description not available] | 0 | 2.08 | 1 | 0 |
CJD (Creutzfeldt-Jakob Disease) [description not available] | 0 | 2.08 | 1 | 0 |
Creutzfeldt-Jakob Syndrome A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27)) | 0 | 2.08 | 1 | 0 |
Meningeal Carcinomatosis Primary or secondary neoplasm in the ARACHNOID or SUBARACHNOID SPACE. It appears as a diffuse fibrotic thickening of the MENINGES associated with variable degrees of inflammation. | 0 | 2.08 | 1 | 0 |
Desmoid [description not available] | 0 | 2.07 | 1 | 0 |
Myofibroma A benign tumor that consists chiefly of fibrous CONNECTIVE TISSUE, with variable numbers of MUSCLE CELLS forming portions of the neoplasm (From Stedman's, 27th ed). | 0 | 2.45 | 2 | 0 |
Fibromatosis, Aggressive A childhood counterpart of abdominal or extra-abdominal desmoid tumors, characterized by firm subcutaneous nodules that grow rapidly in any part of the body but do not metastasize. The adult form of abdominal fibromatosis is FIBROMATOSIS, ABDOMINAL. (Stedman, 25th ed) | 0 | 2.07 | 1 | 0 |
Asymptomatic Conditions [description not available] | 0 | 2.07 | 1 | 0 |
Carcinoma, Verrucous A variant of well-differentiated epidermoid carcinoma that is most common in the oral cavity, but also occurs in the larynx, nasal cavity, esophagus, penis, anorectal region, vulva, vagina, uterine cervix, and skin, especially on the sole of the foot. Most intraoral cases occur in elderly male abusers of smokeless tobacco. The treatment is surgical resection. Radiotherapy is not indicated, as up to 30% treated with radiation become highly aggressive within six months. (Segen, Dictionary of Modern Medicine, 1992) | 0 | 4.01 | 5 | 0 |
Cystadenocarcinoma A malignant neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. The neoplastic cells manifest varying degrees of anaplasia and invasiveness, and local extension and metastases occur. Cystadenocarcinomas develop frequently in the ovaries, where pseudomucinous and serous types are recognized. (Stedman, 25th ed) | 0 | 4.47 | 23 | 0 |
Retinal Pigment Epithelial Detachment [description not available] | 0 | 4.19 | 17 | 0 |
Retinal Detachment Separation of the inner layers of the retina (neural retina) from the pigment epithelium. Retinal detachment occurs more commonly in men than in women, in eyes with degenerative myopia, in aging and in aphakia. It may occur after an uncomplicated cataract extraction, but it is seen more often if vitreous humor has been lost during surgery. (Dorland, 27th ed; Newell, Ophthalmology: Principles and Concepts, 7th ed, p310-12). | 0 | 4.19 | 17 | 0 |
AIDS Seroconversion [description not available] | 0 | 4.01 | 5 | 0 |
HIV Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2. | 0 | 2.07 | 1 | 0 |
Acute Edematous Pancreatitis [description not available] | 0 | 4.2 | 17 | 0 |
Pancreatitis INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. | 0 | 4.2 | 17 | 0 |
Experimental Pneumococcal Meningitis [description not available] | 0 | 2.99 | 1 | 0 |
Bacterial Endocarditides, Subacute [description not available] | 0 | 2.99 | 1 | 0 |
Meningitis, Pneumococcal An acute purulent infection of the meninges and subarachnoid space caused by Streptococcus pneumoniae, most prevalent in children and adults over the age of 60. This illness may be associated with OTITIS MEDIA; MASTOIDITIS; SINUSITIS; RESPIRATORY TRACT INFECTIONS; sickle cell disease (ANEMIA, SICKLE CELL); skull fractures; and other disorders. Clinical manifestations include FEVER; HEADACHE; neck stiffness; and somnolence followed by SEIZURES; focal neurologic deficits (notably DEAFNESS); and COMA. (From Miller et al., Merritt's Textbook of Neurology, 9th ed, p111) | 0 | 2.99 | 1 | 0 |
Anterior Cervical Pain [description not available] | 0 | 2.07 | 1 | 0 |
Neck Pain Discomfort or more intense forms of pain that are localized to the cervical region. This term generally refers to pain in the posterior or lateral regions of the neck. | 0 | 2.07 | 1 | 0 |
Arachnoidal Cerebellar Sarcoma, Circumscribed [description not available] | 0 | 3.08 | 5 | 0 |
Medulloblastoma A malignant neoplasm that may be classified either as a glioma or as a primitive neuroectodermal tumor of childhood (see NEUROECTODERMAL TUMOR, PRIMITIVE). The tumor occurs most frequently in the first decade of life with the most typical location being the cerebellar vermis. Histologic features include a high degree of cellularity, frequent mitotic figures, and a tendency for the cells to organize into sheets or form rosettes. Medulloblastoma have a high propensity to spread throughout the craniospinal intradural axis. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2060-1) | 0 | 3.08 | 5 | 0 |
Preterm Birth [description not available] | 0 | 2.08 | 1 | 0 |
Premature Birth CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION). | 0 | 2.08 | 1 | 0 |
Angioma A vascular anomaly due to proliferation of blood or lymphatic vessels that forms a tumor-like mass. Vessels in the angioma may or may not be dilated. | 0 | 4.13 | 16 | 0 |
Hemangioma A vascular anomaly due to proliferation of BLOOD VESSELS that forms a tumor-like mass. The common types involve CAPILLARIES and VEINS. It can occur anywhere in the body but is most frequently noticed in the SKIN and SUBCUTANEOUS TISSUE. (from Stedman, 27th ed, 2000) | 0 | 4.13 | 16 | 0 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 3.12 | 5 | 0 |
Reperfusion Injury Adverse functional, metabolic, or structural changes in tissues that result from the restoration of blood flow to the tissue (REPERFUSION) following ISCHEMIA. | 0 | 3.12 | 5 | 0 |
Chronic Pancreatitis [description not available] | 0 | 3.65 | 3 | 0 |
Pancreatitis, Chronic INFLAMMATION of the PANCREAS that is characterized by recurring or persistent ABDOMINAL PAIN with or without STEATORRHEA or DIABETES MELLITUS. It is characterized by the irregular destruction of the pancreatic parenchyma which may be focal, segmental, or diffuse. | 0 | 3.65 | 3 | 0 |
Fish Diseases Diseases of freshwater, marine, hatchery or aquarium fish. This term includes diseases of both teleosts (true fish) and elasmobranchs (sharks, rays and skates). | 0 | 2.9 | 4 | 0 |
Infections, RNA Virus [description not available] | 0 | 2.08 | 1 | 0 |
Mucocele A retention cyst of the salivary gland, lacrimal sac, paranasal sinuses, appendix, or gallbladder. (Stedman, 26th ed) | 0 | 2.9 | 4 | 0 |
Sinusitis, Maxillary [description not available] | 0 | 2.46 | 2 | 0 |
Maxillary Sinusitis Inflammation of the NASAL MUCOSA in the MAXILLARY SINUS. In many cases, it is caused by an infection of the bacteria HAEMOPHILUS INFLUENZAE; STREPTOCOCCUS PNEUMONIAE; or STAPHYLOCOCCUS AUREUS. | 0 | 2.46 | 2 | 0 |
Dermatitis Exfoliativa [description not available] | 0 | 4.26 | 7 | 0 |
Dermatitis, Exfoliative The widespread involvement of the skin by a scaly, erythematous dermatitis occurring either as a secondary or reactive process to an underlying cutaneous disorder (e.g., atopic dermatitis, psoriasis, etc.), or as a primary or idiopathic disease. It is often associated with the loss of hair and nails, hyperkeratosis of the palms and soles, and pruritus. (From Dorland, 27th ed) | 0 | 4.26 | 7 | 0 |
Benign Chronic Pemphigus [description not available] | 0 | 3.83 | 4 | 0 |
Arrhythmogenic Right Ventricular Cardiomyopathy [description not available] | 0 | 3 | 1 | 0 |
Arrhythmogenic Right Ventricular Dysplasia A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial cells. Primary injuries usually are at the free wall of right ventricular and right atria resulting in ventricular and supraventricular arrhythmias. | 0 | 3 | 1 | 0 |
Myxoid Liposarcoma [description not available] | 0 | 2.99 | 1 | 0 |
Liposarcoma, Myxoid A liposarcoma containing round mesenchymal cells and a myxoid extracellular matrix in stroma. | 0 | 2.99 | 1 | 0 |
Epididymitis Inflammation of the EPIDIDYMIS. Its clinical features include enlarged epididymis, a swollen SCROTUM; PAIN; PYURIA; and FEVER. It is usually related to infections in the URINARY TRACT, which likely spread to the EPIDIDYMIS through either the VAS DEFERENS or the lymphatics of the SPERMATIC CORD. | 0 | 2.38 | 2 | 0 |
Mouth Breathing Abnormal breathing through the mouth, usually associated with obstructive disorders of the nasal passages. | 0 | 2.1 | 1 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 5.08 | 10 | 0 |
Pleurisy INFLAMMATION of PLEURA, the lining of the LUNG. When PARIETAL PLEURA is involved, there is pleuritic CHEST PAIN. | 0 | 2.41 | 2 | 0 |
AL Amyloidosis [description not available] | 0 | 2.07 | 1 | 0 |
Immunoglobulin Light-chain Amyloidosis A nonproliferative disorder of the PLASMA CELL characterized by excessive production and misfolding of IMMUNOGLOBULIN LIGHT CHAINS that form insoluble amyloid fibrils (see AMYLOID DEPOSITS) in various tissues. Clinical features include LIVER FAILURE; MULTIPLE MYELOMA; NEPHROTIC SYNDROME; RESTRICTIVE CARDIOMYOPATHY, and neuropathies. | 0 | 2.07 | 1 | 0 |
Nevi, Intradermal [description not available] | 0 | 2.08 | 1 | 0 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 2.92 | 4 | 0 |
Hypovolemic [description not available] | 0 | 2.08 | 1 | 0 |
Hypovolemia An abnormally low volume of blood circulating through the body. It may result in hypovolemic shock (see SHOCK). | 0 | 2.08 | 1 | 0 |
Phlegmon [description not available] | 0 | 3.35 | 2 | 0 |
Cellulitis An acute, diffuse, and suppurative inflammation of loose connective tissue, particularly the deep subcutaneous tissues, and sometimes muscle, which is most commonly seen as a result of infection of a wound, ulcer, or other skin lesions. | 0 | 3.35 | 2 | 0 |
Light Sensitivity [description not available] | 0 | 3 | 1 | 0 |
Neurilemoma [description not available] | 0 | 6.33 | 27 | 0 |
Neurilemmoma A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5) | 0 | 6.33 | 27 | 0 |
Zollinger-Ellison Syndrome A syndrome that is characterized by the triad of severe PEPTIC ULCER, hypersecretion of GASTRIC ACID, and GASTRIN-producing tumors of the PANCREAS or other tissue (GASTRINOMA). This syndrome may be sporadic or be associated with MULTIPLE ENDOCRINE NEOPLASIA TYPE 1. | 0 | 2.9 | 4 | 0 |
Goiter Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency (HYPOTHYROIDISM), or hormone overproduction (HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic (GOITER, ENDEMIC). | 0 | 3.38 | 7 | 0 |
Mesothelial Neoplasms [description not available] | 0 | 2.4 | 2 | 0 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 4.09 | 3 | 0 |
Neoplasm Regression, Spontaneous Disappearance of a neoplasm or neoplastic state without the intervention of therapy. | 0 | 2.69 | 3 | 0 |
Besnoitiasis [description not available] | 0 | 2.01 | 1 | 0 |
Intestinal Diseases, Parasitic Infections of the INTESTINES with PARASITES, commonly involving PARASITIC WORMS. Infections with roundworms (NEMATODE INFECTIONS) and tapeworms (CESTODE INFECTIONS) are also known as HELMINTHIASIS. | 0 | 2.01 | 1 | 0 |
Cholangiitis, Sclerosing [description not available] | 0 | 3.09 | 5 | 0 |
Cholangitis, Sclerosing Chronic inflammatory disease of the BILIARY TRACT. It is characterized by fibrosis and hardening of the intrahepatic and extrahepatic biliary ductal systems leading to bile duct strictures, CHOLESTASIS, and eventual BILIARY CIRRHOSIS. | 0 | 3.09 | 5 | 0 |
Cystadenoma A benign neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. In some instances, considerable portions of the neoplasm, or even the entire mass, may be cystic. (Stedman, 25th ed) | 0 | 5.11 | 17 | 0 |
Infections, Parvoviridae [description not available] | 0 | 2.01 | 1 | 0 |
Complications, Infectious Pregnancy [description not available] | 0 | 2.66 | 3 | 0 |
Apnea, Obstructive Sleep [description not available] | 0 | 2.01 | 1 | 0 |
Snoring Rough, noisy breathing during sleep, due to vibration of the uvula and soft palate. | 0 | 2.01 | 1 | 0 |
Sleep Apnea, Obstructive A disorder characterized by recurrent apneas during sleep despite persistent respiratory efforts. It is due to upper airway obstruction. The respiratory pauses may induce HYPERCAPNIA or HYPOXIA. Cardiac arrhythmias and elevation of systemic and pulmonary arterial pressures may occur. Frequent partial arousals occur throughout sleep, resulting in relative SLEEP DEPRIVATION and daytime tiredness. Associated conditions include OBESITY; ACROMEGALY; MYXEDEMA; micrognathia; MYOTONIC DYSTROPHY; adenotonsilar dystrophy; and NEUROMUSCULAR DISEASES. (From Adams et al., Principles of Neurology, 6th ed, p395) | 0 | 2.01 | 1 | 0 |
Blast Phase [description not available] | 0 | 2.01 | 1 | 0 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 2.01 | 1 | 0 |
Blast Crisis An advanced phase of chronic myelogenous leukemia, characterized by a rapid increase in the proportion of immature white blood cells (blasts) in the blood and bone marrow to greater than 30%. | 0 | 2.01 | 1 | 0 |
Leukemia, Myelogenous, Chronic, BCR-ABL Positive Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS. | 0 | 2.01 | 1 | 0 |
Myxoma, Nerve Sheath [description not available] | 0 | 2.01 | 1 | 0 |
Myositis, Multiple [description not available] | 0 | 2.92 | 1 | 0 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 6.09 | 11 | 1 |
Dermatomyositis, Adult Type [description not available] | 0 | 4 | 5 | 0 |
Dermatomyositis A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6) | 0 | 4 | 5 | 0 |
Polymyositis Diseases characterized by inflammation involving multiple muscles. This may occur as an acute or chronic condition associated with medication toxicity (DRUG TOXICITY); CONNECTIVE TISSUE DISEASES; infections; malignant NEOPLASMS; and other disorders. The term polymyositis is frequently used to refer to a specific clinical entity characterized by subacute or slowly progressing symmetrical weakness primarily affecting the proximal limb and trunk muscles. The illness may occur at any age, but is most frequent in the fourth to sixth decade of life. Weakness of pharyngeal and laryngeal muscles, interstitial lung disease, and inflammation of the myocardium may also occur. Muscle biopsy reveals widespread destruction of segments of muscle fibers and an inflammatory cellular response. (Adams et al., Principles of Neurology, 6th ed, pp1404-9) | 0 | 2.92 | 1 | 0 |
Lung Diseases, Interstitial A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of PULMONARY ALVEOLI that extends to the interstitium and beyond leading to diffuse PULMONARY FIBROSIS. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features. | 0 | 6.09 | 11 | 1 |
Polysyndactyly [description not available] | 0 | 2.69 | 3 | 0 |
Infections, Helicobacter [description not available] | 0 | 5.98 | 16 | 0 |
Esophagitis INFLAMMATION, acute or chronic, of the ESOPHAGUS caused by BACTERIA, chemicals, or TRAUMA. | 0 | 2.69 | 3 | 0 |
Helicobacter Infections Infections with organisms of the genus HELICOBACTER, particularly, in humans, HELICOBACTER PYLORI. The clinical manifestations are focused in the stomach, usually the gastric mucosa and antrum, and the upper duodenum. This infection plays a major role in the pathogenesis of type B gastritis and peptic ulcer disease. | 0 | 5.98 | 16 | 0 |
Histiocytic Necrotising Lymphadenitis [description not available] | 0 | 2.41 | 2 | 0 |
Cancer of Pharynx [description not available] | 0 | 5.21 | 19 | 0 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 0 | 5.21 | 19 | 0 |
Lip Diseases Diseases involving the LIP. | 0 | 4.39 | 8 | 0 |
Stomatitis, Denture Inflammation of the mouth due to denture irritation. | 0 | 4.85 | 8 | 1 |
Chronic Hepatitis [description not available] | 0 | 3.69 | 10 | 0 |
Hepatic Failure [description not available] | 0 | 2.71 | 3 | 0 |
Hepatitis, Chronic INFLAMMATION of the LIVER with ongoing hepatocellular injury for 6 months or more, characterized by NECROSIS of HEPATOCYTES and inflammatory cell (LEUKOCYTES) infiltration. Chronic hepatitis can be caused by viruses, medications, autoimmune diseases, and other unknown factors. | 0 | 3.69 | 10 | 0 |
Liver Failure Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed) | 0 | 2.71 | 3 | 0 |
Osteolysis Dissolution of bone that particularly involves the removal or loss of calcium. | 0 | 4.42 | 8 | 0 |
Cervical Dystonia A common form of DYSTONIA due to involuntary sustained or spasmodic, repetitive muscle contractions in the neck region. According to the position of the twisted neck and head, cervical dystonia can be categorized as torticollis, laterocollis, retrocollis, and a combination of these abnormal postures. | 0 | 2.01 | 1 | 0 |
Torticollis A symptom, not a disease, of a twisted neck. In most instances, the head is tipped toward one side and the chin rotated toward the other. The involuntary muscle contractions in the neck region of patients with torticollis can be due to congenital defects, trauma, inflammation, tumors, and neurological or other factors. | 0 | 2.01 | 1 | 0 |
Bilharziasis [description not available] | 0 | 3.07 | 5 | 0 |
Schistosomiasis Infection with flukes (trematodes) of the genus SCHISTOSOMA. Three species produce the most frequent clinical diseases: SCHISTOSOMA HAEMATOBIUM (endemic in Africa and the Middle East), SCHISTOSOMA MANSONI (in Egypt, northern and southern Africa, some West Indies islands, northern 2/3 of South America), and SCHISTOSOMA JAPONICUM (in Japan, China, the Philippines, Celebes, Thailand, Laos). S. mansoni is often seen in Puerto Ricans living in the United States. | 0 | 3.07 | 5 | 0 |
Macular Holes [description not available] | 0 | 3.38 | 7 | 0 |
Retinal Perforations Perforations through the whole thickness of the retina including the macula as the result of inflammation, trauma, degeneration, etc. The concept includes retinal breaks, tears, dialyses, and holes. | 0 | 3.38 | 7 | 0 |
Pink Eye [description not available] | 0 | 2.9 | 4 | 0 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 2.9 | 4 | 0 |
Choriocarcinoma A malignant metastatic form of trophoblastic tumors. Unlike the HYDATIDIFORM MOLE, choriocarcinoma contains no CHORIONIC VILLI but rather sheets of undifferentiated cytotrophoblasts and syncytiotrophoblasts (TROPHOBLASTS). It is characterized by the large amounts of CHORIONIC GONADOTROPIN produced. Tissue origins can be determined by DNA analyses: placental (fetal) origin or non-placental origin (CHORIOCARCINOMA, NON-GESTATIONAL). | 0 | 5.81 | 22 | 0 |
Tuberculoma A tumor-like mass resulting from the enlargement of a tuberculous lesion. | 0 | 2.01 | 1 | 0 |
Injuries, Prenatal [description not available] | 0 | 2.01 | 1 | 0 |
Polyarthritis [description not available] | 0 | 3.6 | 9 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 3.6 | 9 | 0 |
Retinal Degeneration A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304) | 0 | 3.22 | 6 | 0 |
Hypopharyngeal Cancer [description not available] | 0 | 3.6 | 9 | 0 |
Hypopharyngeal Neoplasms Tumors or cancer of the HYPOPHARYNX. | 0 | 3.6 | 9 | 0 |
Bilateral Headache [description not available] | 0 | 4.41 | 3 | 0 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 4.41 | 3 | 0 |
Eye Abnormalities Congenital absence of or defects in structures of the eye; may also be hereditary. | 0 | 2.71 | 3 | 0 |
Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. | 0 | 3.23 | 6 | 0 |
Actinic Reticuloid Syndrome [description not available] | 0 | 4.14 | 6 | 0 |
Islet Cell Tumor, Malignant [description not available] | 0 | 2.7 | 3 | 0 |
Carcinoma, Islet Cell A primary malignant neoplasm of the pancreatic ISLET CELLS. Usually it involves the non-INSULIN-producing cell types, the PANCREATIC ALPHA CELLS and the pancreatic delta cells (SOMATOSTATIN-SECRETING CELLS) in GLUCAGONOMA and SOMATOSTATINOMA, respectively. | 0 | 2.7 | 3 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 4.87 | 8 | 0 |
Acquired Immunodeficiency Syndrome An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993. | 0 | 4.87 | 8 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 2.41 | 2 | 0 |
Dermatitis, Irritant A non-allergic contact dermatitis caused by prolonged exposure to irritants and not explained by delayed hypersensitivity mechanisms. | 0 | 5.33 | 7 | 2 |
Rheumatism [description not available] | 0 | 4.76 | 7 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 4.76 | 7 | 0 |
Thyroid Diseases Pathological processes involving the THYROID GLAND. | 0 | 4.86 | 8 | 1 |
Alcoholic Cirrhosis [description not available] | 0 | 5.07 | 10 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 5.07 | 10 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 2.39 | 2 | 0 |
Cystadenoma, Serous A cystic tumor of the ovary, containing thin, clear, yellow serous fluid and varying amounts of solid tissue, with a malignant potential several times greater than that of mucinous cystadenoma (CYSTADENOMA, MUCINOUS). It can be unilocular, parvilocular, or multilocular. It is often bilateral and papillary. The cysts may vary greatly in size. (Dorland, 27th ed; from Hughes, Obstetric-Gynecologic Terminology, 1972) | 0 | 2.43 | 2 | 0 |
Pars Planitis Form of granulomatous uveitis occurring in the region of the pars plana. This disorder is a common condition with no detectable focal pathology. It causes fibrovascular proliferation at the inferior ora serrata. | 0 | 2.01 | 1 | 0 |
Cancer of Sigmoid [description not available] | 0 | 2.7 | 3 | 0 |
Collagen Diseases Historically, a heterogeneous group of acute and chronic diseases, including rheumatoid arthritis, systemic lupus erythematosus, progressive systemic sclerosis, dermatomyositis, etc. This classification was based on the notion that collagen was equivalent to connective tissue, but with the present recognition of the different types of collagen and the aggregates derived from them as distinct entities, the term collagen diseases now pertains exclusively to those inherited conditions in which the primary defect is at the gene level and affects collagen biosynthesis, post-translational modification, or extracellular processing directly. (From Cecil Textbook of Medicine, 19th ed, p1494) | 0 | 5.98 | 10 | 1 |
Congenital Foot Deformities [description not available] | 0 | 2.01 | 1 | 0 |
Congenital Hand Deformities [description not available] | 0 | 2.01 | 1 | 0 |
Uveitis Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina). (Dorland, 27th ed) | 0 | 3.25 | 6 | 0 |
Bacterial Pneumonia [description not available] | 0 | 2.01 | 1 | 0 |
Actinomyces Infections [description not available] | 0 | 2.42 | 2 | 0 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 2.01 | 1 | 0 |
Pregnancy, Tubal The most common ( | 0 | 3.25 | 6 | 0 |
Choroid Plexus Neoplasms, Primary [description not available] | 0 | 5.57 | 12 | 0 |
Choroid Plexus Neoplasms Benign or malignant tumors which arise from the choroid plexus of the ventricles of the brain. Papillomas (see PAPILLOMA, CHOROID PLEXUS) and carcinomas are the most common histologic subtypes, and tend to seed throughout the ventricular and subarachnoid spaces. Clinical features include headaches, ataxia and alterations of consciousness, primarily resulting from associated HYDROCEPHALUS. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2072; J Neurosurg 1998 Mar;88(3):521-8) | 0 | 5.57 | 12 | 0 |
Breathing Sounds [description not available] | 0 | 3.4 | 1 | 1 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 3.4 | 1 | 1 |
Urinary Tract Diseases [description not available] | 0 | 4.45 | 5 | 1 |
Gout Metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with formation of URIC ACID calculi. | 0 | 3.55 | 3 | 0 |
Corns [description not available] | 0 | 3.89 | 13 | 0 |
Callosities Localized hyperplasia of the horny layer of the epidermis due to pressure or friction. (Dorland, 27th ed) | 0 | 3.89 | 13 | 0 |
Deficiency, Vitamin A [description not available] | 0 | 7.14 | 50 | 0 |
Vitamin A Deficiency A nutritional condition produced by a deficiency of VITAMIN A in the diet, characterized by NIGHT BLINDNESS and other ocular manifestations such as dryness of the conjunctiva and later of the cornea (XEROPHTHALMIA). Vitamin A deficiency is a very common problem worldwide, particularly in developing countries as a consequence of famine or shortages of vitamin A-rich foods. In the United States it is found among the urban poor, the elderly, alcoholics, and patients with malabsorption. (From Cecil Textbook of Medicine, 19th ed, p1179) | 0 | 7.14 | 50 | 0 |
Varices [description not available] | 0 | 2.34 | 2 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 2.34 | 2 | 0 |
Nicotine Addiction [description not available] | 0 | 2.01 | 1 | 0 |
Tobacco Use Disorder Tobacco used to the detriment of a person's health or social functioning. Tobacco dependence is included. | 0 | 2.01 | 1 | 0 |
Lesion of Sciatic Nerve [description not available] | 0 | 2.36 | 2 | 0 |
Viral Diseases [description not available] | 0 | 4.44 | 5 | 0 |
Emphysema A pathological accumulation of air in tissues or organs. | 0 | 1.93 | 1 | 0 |
Vaginitis Inflammation of the vagina characterized by pain and a purulent discharge. | 0 | 1.93 | 1 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 4.44 | 5 | 0 |
Vulvovaginitis Inflammation of the VULVA and the VAGINA, characterized by discharge, burning, and PRURITUS. | 0 | 1.93 | 1 | 0 |
Deficiency, Protein [description not available] | 0 | 2.35 | 2 | 0 |
Elevated Cholesterol [description not available] | 0 | 2.85 | 1 | 0 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 2.85 | 1 | 0 |
Neuroses [description not available] | 0 | 1.93 | 1 | 0 |
Neurotic Disorders Disorders in which the symptoms are distressing to the individual and recognized by him or her as being unacceptable. Social relationships may be greatly affected but usually remain within acceptable limits. The disturbance is relatively enduring or recurrent without treatment. | 0 | 1.93 | 1 | 0 |
Leukokeratosis Leukoplakic lesions related to abnormal keratin fiber formation. | 0 | 5.98 | 27 | 0 |
Leukoplakia A white patch lesion found on a MUCOUS MEMBRANE that cannot be scraped off. Leukoplakia is generally considered a precancerous condition, however its appearance may also result from a variety of HEREDITARY DISEASES. | 0 | 5.98 | 27 | 0 |
Alexander Disease Rare leukoencephalopathy with infantile-onset accumulation of Rosenthal fibers in the subpial, periventricular, and subependymal zones of the brain. Rosenthal fibers are GLIAL FIBRILLARY ACIDIC PROTEIN aggregates found in ASTROCYTES. Juvenile- and adult-onset types show progressive atrophy of the lower brainstem instead. De novo mutations in the GFAP gene are associated with the disease with propensity for paternal inheritance. | 0 | 1.94 | 1 | 0 |
Brain Disorders [description not available] | 0 | 5.46 | 11 | 0 |
Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis [description not available] | 0 | 1.94 | 1 | 0 |
Brain Diseases Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM. | 0 | 5.46 | 11 | 0 |
Lichen Simplex Chronicus [description not available] | 0 | 2.87 | 4 | 0 |
Neurodermatitis An extremely variable eczematous skin disease that is presumed to be a response to prolonged vigorous scratching, rubbing, or pinching to relieve intense pruritus. It varies in intensity, severity, course, and morphologic expression in different individuals. Neurodermatitis is believed by some to be psychogenic. The circumscribed or localized form is often referred to as lichen simplex chronicus. | 0 | 2.87 | 4 | 0 |
Dermatitis, Eczematous [description not available] | 0 | 4.57 | 10 | 0 |
Eczema A pruritic papulovesicular dermatitis occurring as a reaction to many endogenous and exogenous agents (Dorland, 27th ed). | 0 | 4.57 | 10 | 0 |
Frostbite Damage to tissues as the result of low environmental temperatures. | 0 | 2.36 | 2 | 0 |
Chilblains Recurrent localized itching, swelling and painful erythema on the fingers, toes or ears, produced by exposure to cold. | 0 | 1.94 | 1 | 0 |
Nevi, Melanocytic [description not available] | 0 | 5.03 | 16 | 0 |
Nevus, Pigmented A nevus containing melanin. The term is usually restricted to nevocytic nevi (round or oval collections of melanin-containing nevus cells occurring at the dermoepidermal junction of the skin or in the dermis proper) or moles, but may be applied to other pigmented nevi. | 0 | 5.03 | 16 | 0 |
Diseases, Metabolic [description not available] | 0 | 4.43 | 5 | 0 |
Metabolic Diseases Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) | 0 | 4.43 | 5 | 0 |
Abnormalities, Teeth [description not available] | 0 | 3.24 | 6 | 0 |
Sycosis [description not available] | 0 | 3.58 | 9 | 0 |
Folliculitis Inflammation of follicles, primarily hair follicles. | 0 | 3.58 | 9 | 0 |
Graft-Versus-Host Disease [description not available] | 0 | 6.29 | 14 | 1 |
Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION. | 0 | 6.29 | 14 | 1 |
Abortion, Tubal [description not available] | 0 | 4.78 | 7 | 1 |
Hydatid Mole [description not available] | 0 | 3.38 | 7 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 4.78 | 7 | 1 |
Hydatidiform Mole Trophoblastic hyperplasia associated with normal gestation, or molar pregnancy. It is characterized by the swelling of the CHORIONIC VILLI and elevated human CHORIONIC GONADOTROPIN. Hydatidiform moles or molar pregnancy may be categorized as complete or partial based on their gross morphology, histopathology, and karyotype. | 0 | 3.38 | 7 | 0 |
Bone Inflammation [description not available] | 0 | 2.01 | 1 | 0 |
Menopause The last menstrual period. Permanent cessation of menses (MENSTRUATION) is usually defined after 6 to 12 months of AMENORRHEA in a woman over 45 years of age. In the United States, menopause generally occurs in women between 48 and 55 years of age. | 0 | 6.47 | 9 | 0 |
Labor, Premature [description not available] | 0 | 2.01 | 1 | 0 |
Paranasal Sinus Diseases Diseases affecting or involving the PARANASAL SINUSES and generally manifesting as inflammation, abscesses, cysts, or tumors. | 0 | 2.68 | 3 | 0 |
Mediastinal Cyst Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus. | 0 | 3.24 | 6 | 0 |
Vaccinia The cutaneous and occasional systemic reactions associated with vaccination using smallpox (variola) vaccine. | 0 | 2.93 | 1 | 0 |
Eczema Herpeticum [description not available] | 0 | 2.93 | 1 | 0 |
DDD MPGNII [description not available] | 0 | 2.43 | 2 | 0 |
Nephrotic Syndrome A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction. | 0 | 2.41 | 2 | 0 |
Glomerulonephritis, Membranoproliferative Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN. | 0 | 2.43 | 2 | 0 |
Uremia A clinical syndrome associated with the retention of renal waste products or uremic toxins in the blood. It is usually the result of RENAL INSUFFICIENCY. Most uremic toxins are end products of protein or nitrogen CATABOLISM, such as UREA or CREATININE. Severe uremia can lead to multiple organ dysfunctions with a constellation of symptoms. | 0 | 2.02 | 1 | 0 |
Cavernitis, Fibrous [description not available] | 0 | 2.02 | 1 | 0 |
Penile Induration A condition characterized by hardening of the PENIS due to the formation of fibrous plaques on the dorsolateral aspect of the PENIS, usually involving the membrane (tunica albuginea) surrounding the erectile tissue (corpus cavernosum penis). This may eventually cause a painful deformity of the shaft or constriction of the urethra, or both. | 0 | 2.02 | 1 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 6.59 | 19 | 0 |
Carcinoma, Bronchogenic Malignant neoplasm arising from the epithelium of the BRONCHI. It represents a large group of epithelial lung malignancies which can be divided into two clinical groups: SMALL CELL LUNG CANCER and NON-SMALL-CELL LUNG CARCINOMA. | 0 | 6.59 | 19 | 0 |
Monosomy The condition in which one chromosome of a pair is missing. In a normally diploid cell it is represented symbolically as 2N-1. | 0 | 3.61 | 3 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 2.02 | 1 | 0 |
Cytomegalovirus A genus of the family HERPESVIRIDAE, subfamily BETAHERPESVIRINAE, infecting the salivary glands, liver, spleen, lungs, eyes, and other organs, in which they produce characteristically enlarged cells with intranuclear inclusions. Infection with Cytomegalovirus is also seen as an opportunistic infection in AIDS. | 0 | 3.5 | 8 | 0 |
Myocardial Ischemia A disorder of cardiac function caused by insufficient blood flow to the muscle tissue of the heart. The decreased blood flow may be due to narrowing of the coronary arteries (CORONARY ARTERY DISEASE), to obstruction by a thrombus (CORONARY THROMBOSIS), or less commonly, to diffuse narrowing of arterioles and other small vessels within the heart. Severe interruption of the blood supply to the myocardial tissue may result in necrosis of cardiac muscle (MYOCARDIAL INFARCTION). | 0 | 2.02 | 1 | 0 |
Elevated ICP (Intracranial Pressure) [description not available] | 0 | 2.02 | 1 | 0 |
Acrania [description not available] | 0 | 2.94 | 4 | 0 |
Benign Supratentorial Neoplasms [description not available] | 0 | 3.35 | 2 | 0 |
Arachnoid Cysts Intracranial or spinal cavities containing a cerebrospinal-like fluid, the wall of which is composed of arachnoidal cells. They are most often developmental or related to trauma. Intracranial arachnoid cysts usually occur adjacent to arachnoidal cistern and may present with HYDROCEPHALUS; HEADACHE; SEIZURES; and focal neurologic signs. (From Joynt, Clinical Neurology, 1994, Ch44, pp105-115) | 0 | 2.4 | 2 | 0 |
Neural Tube Defects Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41) | 0 | 2.94 | 4 | 0 |
Intracranial Hypertension Increased pressure within the cranial vault. This may result from several conditions, including HYDROCEPHALUS; BRAIN EDEMA; intracranial masses; severe systemic HYPERTENSION; PSEUDOTUMOR CEREBRI; and other disorders. | 0 | 2.02 | 1 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 4.12 | 16 | 0 |
Bladder Disorder, Neurogenic [description not available] | 0 | 2.02 | 1 | 0 |
Urinary Bladder, Neurogenic Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES. | 0 | 2.02 | 1 | 0 |
Amaurosis [description not available] | 0 | 2.69 | 3 | 0 |
Blindness The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; OPTIC CHIASM diseases; or BRAIN DISEASES affecting the VISUAL PATHWAYS or OCCIPITAL LOBE. | 0 | 2.69 | 3 | 0 |
Fibrosis, Radiation [description not available] | 0 | 2.92 | 4 | 0 |
Radiation Pneumonitis Inflammation of the lung due to harmful effects of ionizing or non-ionizing radiation. | 0 | 2.92 | 4 | 0 |
Choline Deficiency A condition produced by a deficiency of CHOLINE in animals. Choline is known as a lipotropic agent because it has been shown to promote the transport of excess fat from the liver under certain conditions in laboratory animals. Combined deficiency of choline (included in the B vitamin complex) and all other methyl group donors causes liver cirrhosis in some animals. Unlike compounds normally considered as vitamins, choline does not serve as a cofactor in enzymatic reactions. (From Saunders Dictionary & Encyclopedia of Laboratory Medicine and Technology, 1984) | 0 | 2.91 | 4 | 0 |
Pyrexia [description not available] | 0 | 2.41 | 2 | 0 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 2.41 | 2 | 0 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 2.68 | 3 | 0 |
Sunburn An injury to the skin causing erythema, tenderness, and sometimes blistering and resulting from excessive exposure to the sun. The reaction is produced by the ultraviolet radiation in sunlight. | 0 | 4.75 | 12 | 0 |
Mediastinal Diseases Disorders of the mediastinum, general or unspecified. | 0 | 2.02 | 1 | 0 |
Bile Duct Obstruction, Intrahepatic [description not available] | 0 | 4.75 | 7 | 1 |
Cholestasis, Intrahepatic Impairment of bile flow due to injury to the HEPATOCYTES; BILE CANALICULI; or the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). | 0 | 4.75 | 7 | 1 |
Glioblastoma with Sarcomatous Component [description not available] | 0 | 2.02 | 1 | 0 |
Gliosarcoma Rare mixed tumors of the brain and rarely the spinal cord which contain malignant neuroectodermal (glial) and mesenchymal components, including spindle-shaped fibrosarcoma cells. These tumors are highly aggressive and present primarily in adults as rapidly expanding mass lesions. They may arise in tissue that has been previously irradiated. (From Br J Neurosurg 1995 Apr;9(2):171-8) | 0 | 2.02 | 1 | 0 |
Salmonella Infections, Animal Infections in animals with bacteria of the genus SALMONELLA. | 0 | 2.02 | 1 | 0 |
Plica Syndrome [description not available] | 0 | 2.41 | 2 | 0 |
Synovitis Inflammation of the SYNOVIAL MEMBRANE. | 0 | 2.41 | 2 | 0 |
Mixed Tumor, Mesodermal A sarcoma of the body of the uterus arising in older women, composed of more than one mesenchymal tissue, especially including striated muscle cells. It is associated with previous pelvic radiation exposure in 20% of patients. (Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1702) | 0 | 2.02 | 1 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 4.76 | 12 | 0 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 2.41 | 2 | 0 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 2.69 | 3 | 0 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 2.69 | 3 | 0 |
Salivary Gland Diseases Diseases involving the SALIVARY GLANDS. | 0 | 3.36 | 7 | 0 |
Infections, Chlamydia [description not available] | 0 | 2.39 | 2 | 0 |
Chlamydia Infections Infections with bacteria of the genus CHLAMYDIA. | 0 | 2.39 | 2 | 0 |
Canine Distemper [description not available] | 0 | 2.02 | 1 | 0 |
Autoimmune Thyroiditis [description not available] | 0 | 4.76 | 7 | 0 |
Viral Hepatitis, Human [description not available] | 0 | 3.24 | 6 | 0 |
Hepatitis, Viral, Human INFLAMMATION of the LIVER in humans due to infection by VIRUSES. There are several significant types of human viral hepatitis with infection caused by enteric-transmission (HEPATITIS A; HEPATITIS E) or blood transfusion (HEPATITIS B; HEPATITIS C; and HEPATITIS D). | 0 | 3.24 | 6 | 0 |
Basedow Disease [description not available] | 0 | 2.9 | 4 | 0 |
Graves Disease A common form of hyperthyroidism with a diffuse hyperplastic GOITER. It is an autoimmune disorder that produces antibodies against the THYROID STIMULATING HORMONE RECEPTOR. These autoantibodies activate the TSH receptor, thereby stimulating the THYROID GLAND and hypersecretion of THYROID HORMONES. These autoantibodies can also affect the eyes (GRAVES OPHTHALMOPATHY) and the skin (Graves dermopathy). | 0 | 2.9 | 4 | 0 |
Gonadal Tissue Neoplasms [description not available] | 0 | 2.91 | 4 | 0 |
Hirsutism A condition observed in WOMEN and CHILDREN when there is excess coarse body hair of an adult male distribution pattern, such as facial and chest areas. It is the result of elevated ANDROGENS from the OVARIES, the ADRENAL GLANDS, or exogenous sources. The concept does not include HYPERTRICHOSIS, which is an androgen-independent excessive hair growth. | 0 | 3.29 | 2 | 0 |
Fisher Syndrome [description not available] | 0 | 2.02 | 1 | 0 |
47,XX,+21 [description not available] | 0 | 3.58 | 3 | 0 |
Breathlessness [description not available] | 0 | 2.02 | 1 | 0 |
Pleuropericarditis Inflammation of both the PERICARDIUM and the PLEURA. | 0 | 2.43 | 2 | 0 |
Down Syndrome A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213) | 0 | 3.58 | 3 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 2.02 | 1 | 0 |
Pericarditis Inflammation of the PERICARDIUM from various origins, such as infection, neoplasm, autoimmune process, injuries, or drug-induced. Pericarditis usually leads to PERICARDIAL EFFUSION, or CONSTRICTIVE PERICARDITIS. | 0 | 2.43 | 2 | 0 |
Ventricular Fibrillation A potentially lethal cardiac arrhythmia that is characterized by uncoordinated extremely rapid firing of electrical impulses (400-600/min) in HEART VENTRICLES. Such asynchronous ventricular quivering or fibrillation prevents any effective cardiac output and results in unconsciousness (SYNCOPE). It is one of the major electrocardiographic patterns seen with CARDIAC ARREST. | 0 | 2.02 | 1 | 0 |
Respiratory Syndrome, Acute, Severe [description not available] | 0 | 2.94 | 4 | 0 |
Aspergillus Infection [description not available] | 0 | 2.02 | 1 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 2.43 | 2 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 4.49 | 9 | 0 |
Fungal Lung Diseases [description not available] | 0 | 3.31 | 2 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 2.02 | 1 | 0 |
Cytomegalovirus Infections Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults. | 0 | 2.43 | 2 | 0 |
Herpes Simplex A group of acute infections caused by herpes simplex virus type 1 or type 2 that is characterized by the development of one or more small fluid-filled vesicles with a raised erythematous base on the skin or mucous membrane. It occurs as a primary infection or recurs due to a reactivation of a latent infection. (Dorland, 27th ed.) | 0 | 4.49 | 9 | 0 |
Severe Acute Respiratory Syndrome A viral disorder characterized by high FEVER, dry COUGH, shortness of breath (DYSPNEA) or breathing difficulties, and atypical PNEUMONIA. A virus in the genus CORONAVIRUS is the suspected agent. | 0 | 2.94 | 4 | 0 |
Hemangiopericytoma A tumor composed of spindle cells with a rich vascular network, which apparently arises from pericytes, cells of smooth muscle origin that lie around small vessels. Benign and malignant hemangiopericytomas exist, and the rarity of these lesions has led to considerable confusion in distinguishing between benign and malignant variants. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1364) | 0 | 4.29 | 7 | 0 |
Blood Poisoning [description not available] | 0 | 2.02 | 1 | 0 |
Sepsis Systemic inflammatory response syndrome with a proven or suspected infectious etiology. When sepsis is associated with organ dysfunction distant from the site of infection, it is called severe sepsis. When sepsis is accompanied by HYPOTENSION despite adequate fluid infusion, it is called SEPTIC SHOCK. | 0 | 2.02 | 1 | 0 |
Infections, Pseudomonas [description not available] | 0 | 2.02 | 1 | 0 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 2.02 | 1 | 0 |
Diseases, Occupational [description not available] | 0 | 3.09 | 5 | 0 |
Arthritis, Juvenile Chronic [description not available] | 0 | 2.69 | 3 | 0 |
Arthritis, Juvenile Arthritis in children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. | 0 | 2.69 | 3 | 0 |
Bronchial Pneumonia [description not available] | 0 | 2.02 | 1 | 0 |
Acute Bacterial Prostatitis [description not available] | 0 | 2.42 | 2 | 0 |
Prostatitis Infiltration of inflammatory cells into the parenchyma of PROSTATE. The subtypes are classified by their varied laboratory analysis, clinical presentation and response to treatment. | 0 | 2.42 | 2 | 0 |
Bovine Spongiform Encephalopathy [description not available] | 0 | 2.02 | 1 | 0 |
Retinal Diseases Diseases involving the RETINA. | 0 | 3.99 | 14 | 0 |
Flank Pain Pain emanating from below the RIBS and above the ILIUM. | 0 | 3.35 | 2 | 0 |
Kidney Stones [description not available] | 0 | 3.31 | 2 | 0 |
Kidney Calculi Stones in the KIDNEY, usually formed in the urine-collecting area of the kidney (KIDNEY PELVIS). Their sizes vary and most contains CALCIUM OXALATE. | 0 | 3.31 | 2 | 0 |
Blood Diseases [description not available] | 0 | 3.34 | 2 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 4.78 | 12 | 0 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 3.34 | 2 | 0 |
Placenta Diseases Pathological processes or abnormal functions of the PLACENTA. | 0 | 2.68 | 3 | 0 |
Neoplasms, Trophoblastic [description not available] | 0 | 3.86 | 12 | 0 |
Placental-Site Trophoblastic Tumor [description not available] | 0 | 3.84 | 4 | 0 |
Trophoblastic Tumor, Placental Site An uncommon variant of CHORIOCARCINOMA. It is composed almost entirely of mononuclear cytotrophoblasts (TROPHOBLASTS). Because its secretion of hCG (CHORIONIC GONADOTROPIN) is low, a large tumor may develop before the hCG can be detected. | 0 | 3.84 | 4 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 2.41 | 2 | 0 |
Sarcoidosis An idiopathic systemic inflammatory granulomatous disorder comprised of epithelioid and multinucleated giant cells with little necrosis. It usually invades the lungs with fibrosis and may also involve lymph nodes, skin, liver, spleen, eyes, phalangeal bones, and parotid glands. | 0 | 2.41 | 2 | 0 |
Sweat Gland Diseases Diseases of the SWEAT GLANDS. | 0 | 4.62 | 6 | 0 |
Reproductive Sterility [description not available] | 0 | 2.02 | 1 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 2.02 | 1 | 0 |
Urinary Tract Infections Inflammatory responses of the epithelium of the URINARY TRACT to microbial invasions. They are often bacterial infections with associated BACTERIURIA and PYURIA. | 0 | 2.66 | 3 | 0 |
Alveolar Soft Part Sarcoma [description not available] | 0 | 2.94 | 1 | 0 |
Sarcoma, Alveolar Soft Part A variety of rare sarcoma having a reticulated fibrous stroma enclosing groups of sarcoma cells, which resemble epithelial cells and are enclosed in alveoli walled with connective tissue. It is a rare tumor, usually occurring between 15 and 35 years of age. It appears in the muscles of the extremities in adults and most commonly in the head and neck regions of children. Though slow-growing, it commonly metastasizes to the lungs, brain, bones, and lymph nodes. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1365) | 0 | 2.94 | 1 | 0 |
Melanoma, Amelanotic An unpigmented malignant melanoma. It is an anaplastic melanoma consisting of cells derived from melanoblasts but not forming melanin. (Dorland, 27th ed; Stedman, 25th ed) | 0 | 4.65 | 6 | 0 |
Genetic Diseases [description not available] | 0 | 6.23 | 13 | 0 |
Moniliasis, Oral [description not available] | 0 | 5.75 | 13 | 0 |
Candidiasis, Oral Infection of the mucous membranes of the mouth by a fungus of the genus CANDIDA. (Dorland, 27th ed) | 0 | 5.75 | 13 | 0 |
Genetic Diseases, Inborn Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. | 0 | 6.23 | 13 | 0 |
Abnormality, Torsion [description not available] | 0 | 2.02 | 1 | 0 |
Genito-urinary Cancer [description not available] | 0 | 4 | 5 | 0 |
Urogenital Neoplasms Tumors or cancer of the UROGENITAL SYSTEM in either the male or the female. | 0 | 4 | 5 | 0 |
Ectopic Ossification [description not available] | 0 | 3.68 | 10 | 0 |
Breast Cyst A fluid-filled closed cavity or sac that is lined by an EPITHELIUM and found in the BREAST. It may appear as a single large cyst in one breast, multifocal, or bilateral in FIBROCYSTIC BREAST DISEASE. | 0 | 2.02 | 1 | 0 |
Cleft Spine [description not available] | 0 | 2.02 | 1 | 0 |
Dermal Sinus [description not available] | 0 | 3.6 | 3 | 0 |
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous [description not available] | 0 | 2.02 | 1 | 0 |
Ovarian Hyperstimulation Syndrome A complication of OVULATION INDUCTION in infertility treatment. It is graded by the severity of symptoms which include OVARY enlargement, multiple OVARIAN FOLLICLES; OVARIAN CYSTS; ASCITES; and generalized EDEMA. The full-blown syndrome may lead to RENAL FAILURE, respiratory distress, and even DEATH. Increased capillary permeability is caused by the vasoactive substances, such as VASCULAR ENDOTHELIAL GROWTH FACTORS, secreted by the overly-stimulated OVARIES. | 0 | 2.02 | 1 | 0 |
Eye Foreign Bodies Inanimate objects that become enclosed in the eye. | 0 | 2.02 | 1 | 0 |
Eye Injuries, Penetrating Deeply perforating or puncturing type intraocular injuries. | 0 | 2.02 | 1 | 0 |
Cirrhoses, Experimental Liver [description not available] | 0 | 2.9 | 4 | 0 |
Injuries, Knee [description not available] | 0 | 2.02 | 1 | 0 |
Knee Injuries Injuries to the knee or the knee joint. | 0 | 2.02 | 1 | 0 |
Carditis [description not available] | 0 | 2.02 | 1 | 0 |
Myocarditis Inflammatory processes of the muscular walls of the heart (MYOCARDIUM) which result in injury to the cardiac muscle cells (MYOCYTES, CARDIAC). Manifestations range from subclinical to sudden death (DEATH, SUDDEN). Myocarditis in association with cardiac dysfunction is classified as inflammatory CARDIOMYOPATHY usually caused by INFECTION, autoimmune diseases, or responses to toxic substances. Myocarditis is also a common cause of DILATED CARDIOMYOPATHY and other cardiomyopathies. | 0 | 2.02 | 1 | 0 |
Infarct [description not available] | 0 | 2.92 | 4 | 0 |
Emesis [description not available] | 0 | 2.02 | 1 | 0 |
Nausea An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses. | 0 | 2.02 | 1 | 0 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 2.02 | 1 | 0 |
Bednar Tumor [description not available] | 0 | 2.02 | 1 | 0 |
Dermatofibrosarcoma A sarcoma of the deep layers of the skin. The tumors are locally aggressive tends to recur but rarely metastatic. It can be classified into variants depending on the cell type tumors are derived from or by its characteristics: Pigmented variant from MELANIN-containing DERMAL DENDRITIC CELLS; Myxoid variant, myxoid STROMAL CELLS; Giant cell variant characterized by GIANT CELLS in the tumors; and Fibrosarcomatous variant chracterized by tumor areas histologically indistinguishable from FIBROSARCOMA. | 0 | 2.02 | 1 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 4.15 | 6 | 0 |
Alzheimer Disease A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57) | 0 | 4.15 | 6 | 0 |
Teratocarcinoma A malignant neoplasm consisting of elements of teratoma with those of embryonal carcinoma or choriocarcinoma, or both. It occurs most often in the testis. (Dorland, 27th ed) | 0 | 2.92 | 4 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 3.62 | 3 | 0 |
Body Weight, Fetal [description not available] | 0 | 2.02 | 1 | 0 |
Back Ache [description not available] | 0 | 2.02 | 1 | 0 |
Pain, Intractable Persistent pain that is refractory to some or all forms of treatment. | 0 | 2.02 | 1 | 0 |
Back Pain Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions. | 0 | 2.02 | 1 | 0 |
Dermatitis, Contact, Phototoxic [description not available] | 0 | 2.94 | 1 | 0 |
Avitaminosis A condition due to a deficiency of one or more essential vitamins. (Dorland, 27th ed) | 0 | 2.02 | 1 | 0 |
Granulomatosis, Wegener's [description not available] | 0 | 2.69 | 3 | 0 |
Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN. | 0 | 2.69 | 3 | 0 |
BH4 Deficiency [description not available] | 0 | 2.66 | 3 | 0 |
Phenylketonurias A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952). | 0 | 2.66 | 3 | 0 |
Hypospermatogenesis [description not available] | 0 | 2.92 | 4 | 0 |
Distorted Hearing [description not available] | 0 | 2.41 | 2 | 0 |
Nerve Root Avulsion [description not available] | 0 | 2.03 | 1 | 0 |
Neuralgia, Sciatic [description not available] | 0 | 2.41 | 2 | 0 |
Radiculopathy Disease involving a spinal nerve root (see SPINAL NERVE ROOTS) which may result from compression related to INTERVERTEBRAL DISK DISPLACEMENT; SPINAL CORD INJURIES; SPINAL DISEASES; and other conditions. Clinical manifestations include radicular pain, weakness, and sensory loss referable to structures innervated by the involved nerve root. | 0 | 2.03 | 1 | 0 |
Sciatica A condition characterized by pain radiating from the back into the buttock and posterior/lateral aspects of the leg. Sciatica may be a manifestation of SCIATIC NEUROPATHY; RADICULOPATHY (involving the SPINAL NERVE ROOTS; L4, L5, S1, or S2, often associated with INTERVERTEBRAL DISK DISPLACEMENT); or lesions of the CAUDA EQUINA. | 0 | 2.41 | 2 | 0 |
EHS Tumor [description not available] | 0 | 3.48 | 8 | 0 |
Cystadenoma, Papillary A benign neoplasm of the ovary. | 0 | 2.7 | 3 | 0 |
Congenital Mesoblastic Nephroma [description not available] | 0 | 2.42 | 2 | 0 |
Anemia, Hypochromic Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393) | 0 | 2.88 | 4 | 0 |
Urinary Incontinence, Stress Involuntary discharge of URINE as a result of physical activities that increase abdominal pressure on the URINARY BLADDER without detrusor contraction or overdistended bladder. The subtypes are classified by the degree of leakage, descent and opening of the bladder neck and URETHRA without bladder contraction, and sphincter deficiency. | 0 | 4.89 | 4 | 0 |
Blood Clot [description not available] | 0 | 2.41 | 2 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 2.41 | 2 | 0 |
Chromosomal Instability An increased tendency to acquire CHROMOSOME ABERRATIONS when various processes involved in chromosome replication, repair, or segregation are dysfunctional. | 0 | 2.02 | 1 | 0 |
Adenocarcinoma, Scirrhous An adenocarcinoma with a hard (Greek skirrhos, hard) structure owing to the formation of dense connective tissue in the stroma. (From Dorland, 27th ed) | 0 | 3.1 | 5 | 0 |
Blastocyst Disintegration [description not available] | 0 | 2.43 | 2 | 0 |
Cocarcinogenesis The combination of two or more different factors in the production of cancer. | 0 | 4.41 | 8 | 0 |
Primary Peritonitis [description not available] | 0 | 2.7 | 3 | 0 |
Hemoperitoneum Accumulations of blood in the PERITONEAL CAVITY due to internal HEMORRHAGE. | 0 | 2.02 | 1 | 0 |
Peritonitis INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. | 0 | 2.7 | 3 | 0 |
Gastritis, Atrophic GASTRITIS with atrophy of the GASTRIC MUCOSA, the GASTRIC PARIETAL CELLS, and the mucosal glands leading to ACHLORHYDRIA. Atrophic gastritis usually progresses from chronic gastritis. | 0 | 2.4 | 2 | 0 |
Erythema Migrans, Lingual [description not available] | 0 | 2.66 | 3 | 0 |
Abortion, Recurrent [description not available] | 0 | 2.91 | 4 | 0 |
Anti-Phospholipid Antibody Syndrome [description not available] | 0 | 2.03 | 1 | 0 |
Abortion, Habitual Three or more consecutive spontaneous abortions. | 0 | 2.91 | 4 | 0 |
Antiphospholipid Syndrome The presence of antibodies directed against phospholipids (ANTIBODIES, ANTIPHOSPHOLIPID). The condition is associated with a variety of diseases, notably systemic lupus erythematosus and other connective tissue diseases, thrombopenia, and arterial or venous thromboses. In pregnancy it can cause abortion. Of the phospholipids, the cardiolipins show markedly elevated levels of anticardiolipin antibodies (ANTIBODIES, ANTICARDIOLIPIN). Present also are high levels of lupus anticoagulant (LUPUS COAGULATION INHIBITOR). | 0 | 2.03 | 1 | 0 |
Arrhythmia [description not available] | 0 | 2.02 | 1 | 0 |
Cardiac Arrest, Sudden [description not available] | 0 | 2.02 | 1 | 0 |
Arrhythmias, Cardiac Any disturbances of the normal rhythmic beating of the heart or MYOCARDIAL CONTRACTION. Cardiac arrhythmias can be classified by the abnormalities in HEART RATE, disorders of electrical impulse generation, or impulse conduction. | 0 | 2.02 | 1 | 0 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 2.02 | 1 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 2.94 | 1 | 0 |
Struma Ovarii A rare teratoid tumor of the ovary composed almost entirely of thyroid tissue, with large follicles containing abundant colloid. Occasionally there are symptoms of hyperthyroidism. 5-10% of struma ovarii become malignant, the only absolute criterion for which is the presence of metastasis. (Dorland, 27th ed; Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.02 | 1 | 0 |
Alcoholic Pancreatitis [description not available] | 0 | 2.03 | 1 | 0 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 3.99 | 14 | 0 |
Gallstone Disease [description not available] | 0 | 2.4 | 2 | 0 |
Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). | 0 | 2.4 | 2 | 0 |
Low Bone Density [description not available] | 0 | 2.03 | 1 | 0 |
Child Development Deviations [description not available] | 0 | 2.03 | 1 | 0 |
Bone Diseases, Metabolic Diseases that affect the METABOLIC PROCESSES of BONE TISSUE. | 0 | 2.03 | 1 | 0 |
Developmental Disabilities Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed) | 0 | 2.03 | 1 | 0 |
Habermann Disease [description not available] | 0 | 2.03 | 1 | 0 |
Ectopic Hormone Syndromes [description not available] | 0 | 2.03 | 1 | 0 |
Oral Submucous Fibrosis Irreversible FIBROSIS of the submucosal tissue of the MOUTH. | 0 | 2.71 | 3 | 0 |
Acquired Encephalocele [description not available] | 0 | 2.7 | 3 | 0 |
Nasal Diseases [description not available] | 0 | 2.41 | 2 | 0 |
Thoracic Neoplasms New abnormal growth of tissue in the THORAX. | 0 | 3.09 | 5 | 0 |
Keratoconjunctivitis Sicca Drying and inflammation of the conjunctiva as a result of insufficient lacrimal secretion. When found in association with XEROSTOMIA and polyarthritis, it is called SJOGREN'S SYNDROME. | 0 | 2.41 | 2 | 0 |
Tracheal Diseases Diseases involving the TRACHEA. | 0 | 2.38 | 2 | 0 |
Bladder Pain Syndrome [description not available] | 0 | 2.71 | 3 | 0 |
Cystitis, Interstitial A condition with recurring discomfort or pain in the URINARY BLADDER and the surrounding pelvic region without an identifiable disease. Severity of pain in interstitial cystitis varies greatly and often is accompanied by increased urination frequency and urgency. | 0 | 2.71 | 3 | 0 |
Angiolymphoid Hyperplasia with Eosinophilia Solitary or multiple benign cutaneous nodules comprised of immature and mature vascular structures intermingled with endothelial cells and a varied infiltrate of eosinophils, histiocytes, lymphocytes, and mast cells. | 0 | 2.03 | 1 | 0 |
Bone Diseases Diseases of BONES. | 0 | 3.07 | 5 | 0 |
Hyperplasia of Thymus Gland [description not available] | 0 | 3.08 | 5 | 0 |
Inborn Errors of Metabolism [description not available] | 0 | 3.81 | 4 | 0 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 3.81 | 4 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 2.91 | 4 | 0 |
Lymphangioma A benign tumor resulting from a congenital malformation of the lymphatic system. Lymphangioendothelioma is a type of lymphangioma in which endothelial cells are the dominant component. | 0 | 2.91 | 4 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 3.58 | 3 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 3.58 | 3 | 0 |
Acquired Facial Neuropathy [description not available] | 0 | 2.03 | 1 | 0 |
Iron Overload An excessive accumulation of iron in the body due to a greater than normal absorption of iron from the gastrointestinal tract or from parenteral injection. This may arise from idiopathic hemochromatosis, excessive iron intake, chronic alcoholism, certain types of refractory anemia, or transfusional hemosiderosis. (From Churchill's Illustrated Medical Dictionary, 1989) | 0 | 2.94 | 1 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 2.03 | 1 | 0 |
Peptic Ulcer Perforation Penetration of a PEPTIC ULCER through the wall of DUODENUM or STOMACH allowing the leakage of luminal contents into the PERITONEAL CAVITY. | 0 | 3.34 | 2 | 0 |
Peptic Ulcer Ulcer that occurs in the regions of the GASTROINTESTINAL TRACT which come into contact with GASTRIC JUICE containing PEPSIN and GASTRIC ACID. It occurs when there are defects in the MUCOSA barrier. The common forms of peptic ulcers are associated with HELICOBACTER PYLORI and the consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 2.03 | 1 | 0 |
Enlarged Liver [description not available] | 0 | 2.03 | 1 | 0 |
Cancer of the Urethra [description not available] | 0 | 3.38 | 7 | 0 |
Urethral Neoplasms Cancer or tumors of the URETHRA. Benign epithelial tumors of the urethra usually consist of squamous and transitional cells. Primary urethral carcinomas are rare and typically of squamous cells. Urethral carcinoma is the only urological malignancy that is more common in females than in males. | 0 | 3.38 | 7 | 0 |
Starvation Lengthy and continuous deprivation of food. (Stedman, 25th ed) | 0 | 3.34 | 2 | 0 |
Anorexia Nervosa An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 2.94 | 1 | 0 |
Acute Membranous Gingivitis [description not available] | 0 | 2.03 | 1 | 0 |
Lymphangiomyomatosis [description not available] | 0 | 2.41 | 2 | 0 |
Lymphangioleiomyomatosis A disease characterized by the progressive invasion of SMOOTH MUSCLE CELLS into the LYMPHATIC VESSELS, and the BLOOD VESSELS. The majority of the cases occur in the LUNGS of women of child-bearing age, eventually blocking the flow of air, blood, and lymph. The common symptom is shortness of breath (DYSPNEA). | 0 | 2.41 | 2 | 0 |
Rupture, Spontaneous Tear or break of an organ, vessel or other soft part of the body, occurring in the absence of external force. | 0 | 3.11 | 5 | 0 |
Cranial Nerve V Diseases [description not available] | 0 | 2.03 | 1 | 0 |
Amyotonia Congenita [description not available] | 0 | 2.94 | 1 | 0 |
Neuromuscular Diseases A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA. | 0 | 2.94 | 1 | 0 |
Abnormalities, Cardiovascular [description not available] | 0 | 2.44 | 2 | 0 |
Cardiovascular Abnormalities Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS. | 0 | 2.44 | 2 | 0 |
Disgerminoma [description not available] | 0 | 4.17 | 17 | 0 |
Dysgerminoma A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646) | 0 | 4.17 | 17 | 0 |
Hemorrhagic Fever, Epidemic [description not available] | 0 | 2.03 | 1 | 0 |
Hemorrhagic Fever with Renal Syndrome An acute febrile disease occurring predominately in Asia. It is characterized by fever, prostration, vomiting, hemorrhagic phenonema, shock, and renal failure. It is caused by any one of several closely related species of the genus Hantavirus. The most severe form is caused by HANTAAN VIRUS whose natural host is the rodent Apodemus agrarius. Milder forms are caused by SEOUL VIRUS and transmitted by the rodents Rattus rattus and R. norvegicus, and the PUUMALA VIRUS with transmission by Clethrionomys galreolus. | 0 | 2.03 | 1 | 0 |
Blastomyces brasiliensis Infection [description not available] | 0 | 2.03 | 1 | 0 |
B. burgdorferi Infection [description not available] | 0 | 2.03 | 1 | 0 |
Lyme Disease An infectious disease caused by a spirochete, BORRELIA BURGDORFERI, which is transmitted chiefly by Ixodes dammini (see IXODES) and pacificus ticks in the United States and Ixodes ricinis (see IXODES) in Europe. It is a disease with early and late cutaneous manifestations plus involvement of the nervous system, heart, eye, and joints in variable combinations. The disease was formerly known as Lyme arthritis and first discovered at Old Lyme, Connecticut. | 0 | 2.03 | 1 | 0 |
Hyperdactyly [description not available] | 0 | 2.03 | 1 | 0 |
Kidney, Polycystic [description not available] | 0 | 3.69 | 10 | 0 |
Polycystic Kidney Diseases Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance. | 0 | 3.69 | 10 | 0 |
Ascites, Gelatinous [description not available] | 0 | 4.62 | 10 | 0 |
Pseudomyxoma Peritonei A peritoneal adenocarcinoma characterized by build-up of MUCUS in the PERITONEAL CAVITY. Mucus secreting cells may attach to the peritoneal lining and continue to secrete mucus. The majority of cases represent tumor spread from a primary low-grade mucinous neoplasm of the APPENDIX (NCI Thesaurus). | 0 | 4.62 | 10 | 0 |
Bullous Dermatoses [description not available] | 0 | 7.37 | 33 | 0 |
Allergic Conjunctivitis [description not available] | 0 | 2.03 | 1 | 0 |
Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | 0 | 2.03 | 1 | 0 |
Interstitial Cell Tumor [description not available] | 0 | 3.48 | 8 | 0 |
Familial Precocious Puberty [description not available] | 0 | 2.03 | 1 | 0 |
Puberty, Precocious Development of SEXUAL MATURATION in boys and girls at a chronological age that is 2.5 standard deviations below the mean age at onset of PUBERTY in the population. This early maturation of the hypothalamic-pituitary-gonadal axis results in sexual precocity, elevated serum levels of GONADOTROPINS and GONADAL STEROID HORMONES such as ESTRADIOL and TESTOSTERONE. | 0 | 2.03 | 1 | 0 |
Phimosis A condition in which the FORESKIN cannot be retracted to reveal the GLANS PENIS. It is due to tightness or narrowing of the foreskin opening. | 0 | 2.68 | 3 | 0 |
Penile Diseases Pathological processes involving the PENIS or its component tissues. | 0 | 3.06 | 5 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura [description not available] | 0 | 2.03 | 1 | 0 |
Purpura, Thrombotic Thrombocytopenic An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases. | 0 | 2.03 | 1 | 0 |
Bruise [description not available] | 0 | 2.03 | 1 | 0 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 2.03 | 1 | 0 |
Overweight A status with BODY WEIGHT that is above certain standards. In the scale of BODY MASS INDEX, overweight is defined as having a BMI of 25.0-29.9 kg/m2. Overweight may or may not be due to increases in body fat (ADIPOSE TISSUE), hence overweight does not equal over fat. | 0 | 2.03 | 1 | 0 |
Alcoholic Fatty Liver [description not available] | 0 | 3.1 | 5 | 0 |
Nails, Ingrown Excessive lateral nail growth into the nail fold. Because the lateral margin of the nail acts as a foreign body, inflammation and granulation may result. It is caused by improperly fitting shoes and by improper trimming of the nail. | 0 | 2.03 | 1 | 0 |
Perforated Appendicitis [description not available] | 0 | 2.03 | 1 | 0 |
Appendicitis Acute inflammation of the APPENDIX. Acute appendicitis is classified as simple, gangrenous, or perforated. | 0 | 2.03 | 1 | 0 |
Dementias, Transmissible [description not available] | 0 | 2.03 | 1 | 0 |
Pulmonary Consumption [description not available] | 0 | 2.89 | 4 | 0 |
Granuloma, Plasma Cell, Pulmonary [description not available] | 0 | 2.03 | 1 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 2.89 | 4 | 0 |
Chylopericardium [description not available] | 0 | 2.69 | 3 | 0 |
Pericardial Effusion Fluid accumulation within the PERICARDIUM. Serous effusions are associated with pericardial diseases. Hemopericardium is associated with trauma. Lipid-containing effusion (chylopericardium) results from leakage of THORACIC DUCT. Severe cases can lead to CARDIAC TAMPONADE. | 0 | 2.69 | 3 | 0 |
Cancer Syndromes, Hereditary [description not available] | 0 | 3.32 | 2 | 0 |
Sclera Diseases [description not available] | 0 | 2.42 | 2 | 0 |
Mesenchymoma A mixed mesenchymal tumor composed of two or more mesodermal cellular elements not commonly associated, not counting fibrous tissue as one of the elements. Mesenchymomas are widely distributed in the body and about 75% are malignant. (Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1866) | 0 | 5.07 | 10 | 0 |
Bile Duct Cysts [description not available] | 0 | 2.03 | 1 | 0 |
Anus Diseases Diseases involving the ANUS. | 0 | 2.4 | 2 | 0 |
Fibrocartilaginous Dysplasia of Bone [description not available] | 0 | 4.92 | 5 | 0 |
Fibrous Dysplasia of Bone A disease of bone marked by thinning of the cortex by fibrous tissue containing bony spicules, producing pain, disability, and gradually increasing deformity. Only one bone may be involved (FIBROUS DYSPLASIA, MONOSTOTIC) or several (FIBROUS DYSPLASIA, POLYOSTOTIC). | 0 | 4.92 | 5 | 0 |
Endolymphatic Stromal Myosis [description not available] | 0 | 2.04 | 1 | 0 |
Sickle Cell Trait The condition of being heterozygous for hemoglobin S. | 0 | 2.42 | 2 | 0 |
Necrotizing Sialometaplasia [description not available] | 0 | 2.03 | 1 | 0 |
Cancer of Parathyroid [description not available] | 0 | 2.69 | 3 | 0 |
Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES. | 0 | 2.03 | 1 | 0 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 2.69 | 3 | 0 |
ACTH-Producing Pituitary Adenoma [description not available] | 0 | 2.03 | 1 | 0 |
Anal Fistula [description not available] | 0 | 2.03 | 1 | 0 |
Leukemia P388 An experimental lymphocytic leukemia originally induced in DBA/2 mice by painting with methylcholanthrene. | 0 | 2.03 | 1 | 0 |
Situs Inversus A congenital abnormality in which organs in the THORAX and the ABDOMEN are opposite to their normal positions (situs solitus) due to lateral transposition. Normally the STOMACH and SPLEEN are on the left, LIVER on the right, the three-lobed right lung is on the right, and the two-lobed left lung on the left. Situs inversus has a familial pattern and has been associated with a number of genes related to microtubule-associated proteins. | 0 | 2.03 | 1 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 4.01 | 5 | 0 |
Oligodendroglioma A relatively slow-growing glioma that is derived from oligodendrocytes and tends to occur in the cerebral hemispheres, thalamus, or lateral ventricle. They may present at any age, but are most frequent in the third to fifth decades, with an earlier incidence peak in the first decade. Histologically, these tumors are encapsulated, relatively avascular, and tend to form cysts and microcalcifications. Neoplastic cells tend to have small round nuclei surrounded by unstained nuclei. The tumors may vary from well-differentiated to highly anaplastic forms. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2052; Adams et al., Principles of Neurology, 6th ed, p655) | 0 | 4.01 | 5 | 0 |
Microglossia [description not available] | 0 | 2.69 | 3 | 0 |
Adamantiades-Behcet Disease [description not available] | 0 | 3.3 | 2 | 0 |
Behcet Syndrome Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well. | 0 | 3.3 | 2 | 0 |
Limited Scleroderma [description not available] | 0 | 2.03 | 1 | 0 |
Scleroderma, Limited The least progressive form of SYSTEMIC SCLERODERMA with skin thickening restricted to the face, neck and areas distal to the elbows and/or knees, sparing the trunk. The CREST SYNDROME is a form of limited scleroderma. | 0 | 2.03 | 1 | 0 |
Ganglioneuroblastoma A moderately malignant neoplasm composed of primitive neuroectodermal cells dispersed in myxomatous or fibrous stroma intermixed with mature ganglion cells. It may undergo transformation into a neuroblastoma. It arises from the sympathetic trunk or less frequently from the adrenal medulla, cerebral cortex, and other locations. Cervical ganglioneuroblastomas may be associated with HORNER SYNDROME and the tumor may occasionally secrete vasoactive intestinal peptide, resulting in chronic diarrhea. | 0 | 2.04 | 1 | 0 |
Submandibular Gland Diseases Diseases involving the SUBMANDIBULAR GLAND. | 0 | 3.23 | 6 | 0 |
Teeth, Unerupted [description not available] | 0 | 2.04 | 1 | 0 |
Choroid Neoplasms Tumors of the choroid; most common intraocular tumors are malignant melanomas of the choroid. These usually occur after puberty and increase in incidence with advancing age. Most malignant melanomas of the uveal tract develop from benign melanomas (nevi). | 0 | 4.3 | 7 | 0 |
Choroiditis Inflammation of the choroid. | 0 | 2.04 | 1 | 0 |
Angiomatosis A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS, or reactive vascular proliferations, such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic. | 0 | 2.68 | 3 | 0 |
Hyperidrosis [description not available] | 0 | 2.4 | 2 | 0 |
Hyperhidrosis Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief cause is thought to be emotional. Generalized hyperhidrosis may be induced by a hot, humid environment, by fever, or by vigorous exercise. | 0 | 2.4 | 2 | 0 |
Degenerative Disease, Nervous System, Hereditary [description not available] | 0 | 2.96 | 1 | 0 |
Nervous System Disorders [description not available] | 0 | 4.07 | 3 | 0 |
Taste Disorder, Anterior Tongue [description not available] | 0 | 2.96 | 1 | 0 |
Nervous System Diseases Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle. | 0 | 4.07 | 3 | 0 |
Avian Flu [description not available] | 0 | 2.04 | 1 | 0 |
Grippe [description not available] | 0 | 2.04 | 1 | 0 |
Influenza in Birds Infection of domestic and wild fowl and other BIRDS with INFLUENZA A VIRUS. Avian influenza usually does not sicken birds, but can be highly pathogenic and fatal in domestic POULTRY. | 0 | 2.04 | 1 | 0 |
Influenza, Human An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia. | 0 | 2.04 | 1 | 0 |
Extramembranous Glomerulopathy [description not available] | 0 | 2.04 | 1 | 0 |
Glomerulonephritis, Membranous A type of glomerulonephritis that is characterized by the accumulation of immune deposits (COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of the GLOMERULAR BASEMENT MEMBRANE. It progresses from subepithelial dense deposits, to basement membrane reaction and eventual thickening of the basement membrane. | 0 | 2.04 | 1 | 0 |
Rhabdomyosarcoma 2 [description not available] | 0 | 2.04 | 1 | 0 |
Rhabdomyosarcoma, Alveolar A form of RHABDOMYOSARCOMA occurring mainly in adolescents and young adults, affecting muscles of the extremities, trunk, orbital region, etc. It is extremely malignant, metastasizing widely at an early stage. Few cures have been achieved and the prognosis is poor. Alveolar refers to its microscopic appearance simulating the cells of the respiratory alveolus. (Holland et al., Cancer Medicine, 3d ed, p2188) | 0 | 2.04 | 1 | 0 |
Ear Infection [description not available] | 0 | 1.94 | 1 | 0 |
Cerebral Nocardiosis [description not available] | 0 | 1.94 | 1 | 0 |
Maggot Infestations [description not available] | 0 | 1.96 | 1 | 0 |
Apudoma A general term collectively applied to tumors associated with the APUD CELLS series, irrespective of their specific identification. | 0 | 3.07 | 5 | 0 |
Neoplasms, Nervous System [description not available] | 0 | 4.74 | 7 | 0 |
Contact Dermatitis [description not available] | 0 | 5.75 | 21 | 0 |
Dermatitis, Contact A type of acute or chronic skin reaction in which sensitivity is manifested by reactivity to materials or substances coming in contact with the skin. It may involve allergic or non-allergic mechanisms. | 0 | 5.75 | 21 | 0 |
Erythroderma, Sezary [description not available] | 0 | 2.66 | 3 | 0 |
Sezary Syndrome A form of cutaneous T-cell lymphoma manifested by generalized exfoliative ERYTHRODERMA; PRURITUS; peripheral lymphadenopathy, and abnormal hyperchromatic mononuclear (cerebriform) cells in the skin, LYMPH NODES, and peripheral blood (Sezary cells). | 0 | 2.66 | 3 | 0 |
Pemphigoid [description not available] | 0 | 5.43 | 15 | 0 |
Pemphigoid, Bullous A chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. | 0 | 5.43 | 15 | 0 |
Cholangioma [description not available] | 0 | 5.61 | 18 | 0 |
Adenoma, Bile Duct A benign tumor of the intrahepatic bile ducts. | 0 | 5.61 | 18 | 0 |
Abdominal Cramps [description not available] | 0 | 1.96 | 1 | 0 |
Pityriasis Rubra Pilaris A chronic skin disease characterized by small follicular papules, disseminated reddish-brown scaly patches, and often, palmoplantar hyperkeratosis. The papules are about the size of a pin and topped by a horny plug. | 0 | 4.13 | 6 | 0 |
Brain Inflammation [description not available] | 0 | 1.96 | 1 | 0 |
Encephalitis Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition. | 0 | 1.96 | 1 | 0 |
Abnormalities, Sex Chromosome [description not available] | 0 | 2.65 | 3 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 1.96 | 1 | 0 |
Waldenstrom Macroglobulinemia A lymphoproliferative disorder characterized by pleomorphic B-LYMPHOCYTES including PLASMA CELLS, with increased levels of monoclonal serum IMMUNOGLOBULIN M. There is lymphoplasmacytic cells infiltration into bone marrow and often other tissues, also known as lymphoplasmacytic lymphoma. Clinical features include ANEMIA; HEMORRHAGES; and hyperviscosity. | 0 | 1.96 | 1 | 0 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 2.37 | 2 | 0 |
Pneumothorax An accumulation of air or gas in the PLEURAL CAVITY, which may occur spontaneously or as a result of trauma or a pathological process. The gas may also be introduced deliberately during PNEUMOTHORAX, ARTIFICIAL. | 0 | 2.37 | 2 | 0 |
Erythema Multiforme A skin and mucous membrane disease characterized by an eruption of macules, papules, nodules, vesicles, and/or bullae with characteristic bull's-eye lesions usually occurring on the dorsal aspect of the hands and forearms. | 0 | 2.36 | 2 | 0 |
Pityriasis A name originally applied to a group of skin diseases characterized by the formation of fine, branny scales, but now used only with a modifier. (Dorland, 27th ed) | 0 | 2.65 | 3 | 0 |
Clasp-Knife Spasticity [description not available] | 0 | 1.96 | 1 | 0 |
Palsy [description not available] | 0 | 1.96 | 1 | 0 |
Muscle Spasticity A form of muscle hypertonia associated with upper MOTOR NEURON DISEASE. Resistance to passive stretch of a spastic muscle results in minimal initial resistance (a free interval) followed by an incremental increase in muscle tone. Tone increases in proportion to the velocity of stretch. Spasticity is usually accompanied by HYPERREFLEXIA and variable degrees of MUSCLE WEAKNESS. (From Adams et al., Principles of Neurology, 6th ed, p54) | 0 | 1.96 | 1 | 0 |
Paralysis A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) | 0 | 1.96 | 1 | 0 |
Amino Acid Metabolism Disorders, Inborn [description not available] | 0 | 3.56 | 3 | 0 |
Adult Refsum Disease [description not available] | 0 | 4.35 | 3 | 0 |
Kaposi Disease [description not available] | 0 | 4.26 | 7 | 0 |
Acrodermatitis Inflammation involving the skin of the extremities, especially the hands and feet. Several forms are known, some idiopathic and some hereditary. The infantile form is called Gianotti-Crosti syndrome. | 0 | 3.79 | 4 | 0 |
Xeroderma Pigmentosum A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA. | 0 | 4.26 | 7 | 0 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 2.37 | 2 | 0 |
Purpura Purplish or brownish red discoloration, easily visible through the epidermis, caused by hemorrhage into the tissues. When the size of the discolorization is | 0 | 2.37 | 2 | 0 |
Thyroiditis Inflammatory diseases of the THYROID GLAND. Thyroiditis can be classified into acute (THYROIDITIS, SUPPURATIVE), subacute (granulomatous and lymphocytic), chronic fibrous (Riedel's), chronic lymphocytic (HASHIMOTO DISEASE), transient (POSTPARTUM THYROIDITIS), and other AUTOIMMUNE THYROIDITIS subtypes. | 0 | 2.88 | 4 | 0 |
Arthropathies [description not available] | 0 | 3.46 | 8 | 0 |
Joint Diseases Diseases involving the JOINTS. | 0 | 3.46 | 8 | 0 |
Infant, Newborn, Diseases Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts. | 0 | 2.86 | 4 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 3.68 | 10 | 0 |
Hodgkin Disease A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen. | 0 | 3.68 | 10 | 0 |
Alcoholic Hepatitis [description not available] | 0 | 4.74 | 7 | 0 |
Hepatitis, Alcoholic INFLAMMATION of the LIVER due to ALCOHOL ABUSE. It is characterized by NECROSIS of HEPATOCYTES, infiltration by NEUTROPHILS, and deposit of MALLORY BODIES. Depending on its severity, the inflammatory lesion may be reversible or progress to LIVER CIRRHOSIS. | 0 | 4.74 | 7 | 0 |
Vitiligo A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. | 0 | 3.21 | 6 | 0 |
Benign Brenner Tumor [description not available] | 0 | 3.48 | 8 | 0 |
Electric Injuries Injuries caused by electric currents. The concept excludes electric burns (BURNS, ELECTRIC), but includes accidental electrocution and electric shock. | 0 | 1.96 | 1 | 0 |
Adenoma, beta-Cell [description not available] | 0 | 3.08 | 5 | 0 |
Island Cell Tumor [description not available] | 0 | 3.57 | 3 | 0 |
Insulinoma A benign tumor of the PANCREATIC BETA CELLS. Insulinoma secretes excess INSULIN resulting in HYPOGLYCEMIA. | 0 | 3.08 | 5 | 0 |
Adenoma, Islet Cell A benign tumor of the pancreatic ISLET CELLS. Usually it involves the INSULIN-producing PANCREATIC BETA CELLS, as in INSULINOMA, resulting in HYPERINSULINISM. | 0 | 3.57 | 3 | 0 |
Chloasma [description not available] | 0 | 3.22 | 6 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 3.22 | 6 | 0 |
Intestinal Polyps Discrete abnormal tissue masses that protrude into the lumen of the INTESTINE. A polyp is attached to the intestinal wall either by a stalk, pedunculus, or by a broad base. | 0 | 3.58 | 3 | 0 |
Vascular Diseases Pathological processes involving any of the BLOOD VESSELS in the cardiac or peripheral circulation. They include diseases of ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 3.59 | 3 | 0 |
Leukemia, Lymphocytic [description not available] | 0 | 2.37 | 2 | 0 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 2.37 | 2 | 0 |
Leukoedema, Oral A disorder of the buccal mucosa resembling early leukoplakia, characterized by the presence of filmy opalescence of the mucosa in the early stages to a whitish gray cast with a coarsely wrinkled surface in the later stages, associated with intracellular edema of the spinous or malpighian layer. (Dorland, 27th ed) | 0 | 3.28 | 2 | 0 |
Adrenal Gland Hyperfunction [description not available] | 0 | 1.96 | 1 | 0 |
Adenoma, Basophil A small tumor of the anterior lobe of the pituitary gland whose cells stain with basic dyes. It may give rise to excessive secretion of ACTH, resulting in CUSHING SYNDROME. (Dorland, 27th ed) | 0 | 1.96 | 1 | 0 |
Adrenocortical Hyperfunction Excess production of ADRENAL CORTEX HORMONES such as ALDOSTERONE; HYDROCORTISONE; DEHYDROEPIANDROSTERONE; and/or ANDROSTENEDIONE. Hyperadrenal syndromes include CUSHING SYNDROME; HYPERALDOSTERONISM; and VIRILISM. | 0 | 1.96 | 1 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 1.96 | 1 | 0 |
Vitamin D Deficiency A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406) | 0 | 1.96 | 1 | 0 |
Hemorrhage, Oral [description not available] | 0 | 1.96 | 1 | 0 |
Lupus Erythematosus, Chronic Cutaneous [description not available] | 0 | 6.41 | 16 | 1 |
Lupus Erythematosus, Discoid A chronic form of cutaneous lupus erythematosus (LUPUS ERYTHEMATOSUS, CUTANEOUS) in which the skin lesions mimic those of the systemic form but in which systemic signs are rare. It is characterized by the presence of discoid skin plaques showing varying degrees of edema, erythema, scaliness, follicular plugging, and skin atrophy. Lesions are surrounded by an elevated erythematous border. The condition typically involves the face and scalp, but widespread dissemination may occur. | 0 | 6.41 | 16 | 1 |
Aggressive Periodontitis Inflammation and loss of PERIODONTIUM that is characterized by rapid attachment loss and bone destruction in the presence of little local factors such as DENTAL PLAQUE and DENTAL CALCULUS. This highly destructive form of periodontitis often occurs in young people and was called early-onset periodontitis, but this disease also appears in old people. | 0 | 2.67 | 3 | 0 |
Diffuse Tenosynovial Giant Cell Tumor [description not available] | 0 | 2.38 | 2 | 0 |
Synovitis, Pigmented Villonodular Diffuse outgrowth arising from the SYNOVIAL MEMBRANE; SYNOVIAL BURSA; or TENDON sheath around the joint cavity, with extension to surrounding soft tissue. It is characterized by pigmented HEMOSIDERIN-containing MACROPHAGES; FOAM CELLS; and multinucleated GIANT CELLS. It usually occurs in the hands and feet, and around large joints, such as in the ankle and knee joints. | 0 | 2.38 | 2 | 0 |
Acquired Autoimmune Hemolytic Anemia [description not available] | 0 | 1.96 | 1 | 0 |
Anemia, Hemolytic, Autoimmune Acquired hemolytic anemia due to the presence of AUTOANTIBODIES which agglutinate or lyse the patient's own RED BLOOD CELLS. | 0 | 1.96 | 1 | 0 |
Lipidoses Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. | 0 | 3.56 | 3 | 0 |
Caprine Diseases [description not available] | 0 | 2.68 | 3 | 0 |
Brain Ventricular Neoplasms [description not available] | 0 | 4.22 | 18 | 0 |
Coenuri Infection [description not available] | 0 | 1.98 | 1 | 0 |
Liver Diseases, Parasitic Liver diseases caused by infections with PARASITES, such as tapeworms (CESTODA) and flukes (TREMATODA). | 0 | 2.4 | 2 | 0 |
Cysticercosis Infection with CYSTICERCUS, the larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS. | 0 | 1.98 | 1 | 0 |
Autosomal Chromosome Disorders [description not available] | 0 | 5.44 | 15 | 0 |
Anodontia Congenital absence of the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the deciduous and the permanent dentition, or only teeth of the permanent dentition. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Diastema An abnormal opening or fissure between two adjacent teeth. | 0 | 2.37 | 2 | 0 |
Chondrosarcoma, Mesenchymal A rare aggressive variant of chondrosarcoma, characterized by a biphasic histologic pattern of small compact cells intermixed with islands of cartilaginous matrix. Mesenchymal chondrosarcomas have a predilection for flat bones; long tubular bones are rarely affected. They tend to occur in the younger age group and are highly metastatic. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1456) | 0 | 3.3 | 2 | 0 |
Epidermolysis Bullosa Junctionalis, Disentis Type [description not available] | 0 | 4.47 | 5 | 0 |
Epidermolysis Bullosa, Junctional Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterized by generalized blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane. | 0 | 4.47 | 5 | 0 |
Pleural Diseases Diseases involving the PLEURA. | 0 | 2.66 | 3 | 0 |
Hypesthesia Absent or reduced sensitivity to cutaneous stimulation. | 0 | 1.98 | 1 | 0 |
Female Genital Diseases [description not available] | 0 | 2.89 | 4 | 0 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 2.89 | 4 | 0 |
Adenoma, Chromophobe A benign tumor of the anterior pituitary in which the cells do not stain with acidic or basic dyes. | 0 | 2.38 | 2 | 0 |
Adenoma, Acidophil A benign tumor, usually found in the anterior lobe of the pituitary gland, whose cells stain with acid dyes. Such pituitary tumors may give rise to excessive secretion of growth hormone, resulting in gigantism or acromegaly. A specific type of acidophil adenoma may give rise to nonpuerperal galactorrhea. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Impotence [description not available] | 0 | 1.98 | 1 | 0 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 1.98 | 1 | 0 |
Choroid Diseases Disorders of the choroid including hereditary choroidal diseases, neoplasms, and other abnormalities of the vascular layer of the uvea. | 0 | 1.98 | 1 | 0 |
Edema, Fetal [description not available] | 0 | 2.39 | 2 | 0 |
Arsenic Encephalopathy [description not available] | 0 | 1.98 | 1 | 0 |
Poisoning Used with drugs, chemicals, and industrial materials for human or animal poisoning, acute or chronic, whether the poisoning is accidental, occupational, suicidal, by medication error, or by environmental exposure. | 0 | 2.39 | 2 | 0 |
Ectopic Pregnancy [description not available] | 0 | 2.9 | 4 | 0 |
Pregnancy, Ectopic A potentially life-threatening condition in which EMBRYO IMPLANTATION occurs outside the cavity of the UTERUS. Most ectopic pregnancies ( | 0 | 2.9 | 4 | 0 |
Adjuvant Arthritis [description not available] | 0 | 2.39 | 2 | 0 |
Prurigo A name applied to several itchy skin eruptions of unknown cause. The characteristic course is the formation of a dome-shaped papule with a small transient vesicle on top, followed by crusting over or lichenification. (From Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Abortion, Incomplete Premature loss of PREGNANCY in which not all the products of CONCEPTION have been expelled. | 0 | 1.98 | 1 | 0 |
Ankylosing Spondylarthritis [description not available] | 0 | 3.3 | 2 | 0 |
Psoriasis Arthropathica [description not available] | 0 | 1.98 | 1 | 0 |
Arthritis, Post-Infectious [description not available] | 0 | 1.98 | 1 | 0 |
Spondylitis, Ankylosing A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions. | 0 | 3.3 | 2 | 0 |
Arthritis, Psoriatic A type of inflammatory arthritis associated with PSORIASIS, often involving the axial joints and the peripheral terminal interphalangeal joints. It is characterized by the presence of HLA-B27-associated SPONDYLARTHROPATHY, and the absence of rheumatoid factor. | 0 | 1.98 | 1 | 0 |
Arthritis, Reactive An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN. | 0 | 1.98 | 1 | 0 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 2.39 | 2 | 0 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 3.07 | 5 | 0 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 2.68 | 3 | 0 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 2.68 | 3 | 0 |
Granulocytic Leukemia [description not available] | 0 | 2.9 | 4 | 0 |
Leukemia, Myeloid Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites. | 0 | 2.9 | 4 | 0 |
Leukemia, Pre-B-Cell [description not available] | 0 | 1.98 | 1 | 0 |
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma A leukemia/lymphoma found predominately in children and adolescents and characterized by a high number of lymphoblasts and solid tumor lesions. Frequent sites involve LYMPH NODES, skin, and bones. It most commonly presents as leukemia. | 0 | 1.98 | 1 | 0 |
Lentiginosis, Perioral [description not available] | 0 | 1.98 | 1 | 0 |
Peutz-Jeghers Syndrome A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits. | 0 | 1.98 | 1 | 0 |
Otitis Media, Purulent [description not available] | 0 | 1.98 | 1 | 0 |
Otitis Media, Suppurative Inflammation of the middle ear with purulent discharge. | 0 | 1.98 | 1 | 0 |
Gonadoblastoma A complex neoplasm composed of a mixture of gonadal elements, such as large primordial GERM CELLS, immature SERTOLI CELLS or GRANULOSA CELLS of the sex cord, and gonadal stromal cells. Gonadoblastomas are most often associated with gonadal dysgenesis, 46, XY. | 0 | 1.98 | 1 | 0 |
Neoplasms, Nerve Tissue Neoplasms composed of nerve tissue. This concept does not refer to neoplasms located in the nervous system or its component nerves. | 0 | 3.58 | 3 | 0 |
Neurofibroma A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016) | 0 | 2.88 | 4 | 0 |
Sterility, Female [description not available] | 0 | 2.39 | 2 | 0 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 2.39 | 2 | 0 |
Mesothelioma, Cystic A peritoneal mesothelioma affecting mainly young females and producing cysts of variable size and number lined by a single layer of benign mesothelial cells. The disease follows a benign course and is compatible with a normal life expectancy, requiring occasionally partial excision or decompression for relief of pain or other symptoms. Malignant potential is exceptional. (From Holland et al., Cancer Medicine, 3d ed, p1345) | 0 | 3.09 | 5 | 0 |
Mucoepidermoid Tumor A malignant epithelial tumor of glandular tissue, especially the salivary glands, characterized by acini with mucus-producing cells and by the presence of malignant squamous elements. Most mucoepidermoid tumors are low-grade lesions readily cured by adequate excision. They may appear in any age group. They grow slowly. If high-grade, they behave aggressively, widely infiltrating the salivary gland and producing lymph node and distant metastases. (Dorland, 27th ed; from DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p575) | 0 | 2.9 | 1 | 0 |
Hemorrhage, Subarachnoid [description not available] | 0 | 2.39 | 2 | 0 |
Hemorrhage, Vitreous [description not available] | 0 | 1.98 | 1 | 0 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 2.39 | 2 | 0 |
Vitreous Hemorrhage Hemorrhage into the VITREOUS BODY. | 0 | 1.98 | 1 | 0 |
Glandular Fever [description not available] | 0 | 2.66 | 3 | 0 |
Infectious Mononucleosis A common, acute infection usually caused by the Epstein-Barr virus (HERPESVIRUS 4, HUMAN). There is an increase in mononuclear white blood cells and other atypical lymphocytes, generalized lymphadenopathy, splenomegaly, and occasionally hepatomegaly with hepatitis. | 0 | 2.66 | 3 | 0 |
Infections, Respiratory [description not available] | 0 | 2.67 | 3 | 0 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 2.67 | 3 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 2.39 | 2 | 0 |
Adenomatous Polyps Benign neoplasms derived from glandular epithelium. (From Stedman, 25th ed) | 0 | 2.68 | 3 | 0 |
Autolysis The spontaneous disintegration of tissues or cells by the action of their own autogenous enzymes. | 0 | 3.2 | 6 | 0 |
Adenoma, Hepatocellular [description not available] | 0 | 2.69 | 3 | 0 |
Lymphangitis A lymphatic disease characterized by INFLAMMATION of LYMPHATIC VESSELS. | 0 | 2.4 | 2 | 0 |
Infectious Diseases [description not available] | 0 | 2.39 | 2 | 0 |
Communicable Diseases An illness caused by an infectious agent or its toxins that occurs through the direct or indirect transmission of the infectious agent or its products from an infected individual or via an animal, vector or the inanimate environment to a susceptible animal or human host. | 0 | 2.39 | 2 | 0 |
AIDS, Simian [description not available] | 0 | 2.39 | 2 | 0 |
Primate Diseases Diseases of animals within the order PRIMATES. This term includes diseases of Haplorhini and Strepsirhini. | 0 | 1.98 | 1 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 3.78 | 11 | 0 |
Onchocerciasis Infection with nematodes of the genus ONCHOCERCA. Characteristics include the presence of firm subcutaneous nodules filled with adult worms, PRURITUS, and ocular lesions. | 0 | 6.27 | 9 | 0 |
Factitious Disorders Disorders characterized by physical or psychological symptoms that are not real, genuine, or natural. | 0 | 1.98 | 1 | 0 |
Bacterial Skin Diseases [description not available] | 0 | 1.98 | 1 | 0 |
Corynebacterium Infections Infections with bacteria of the genus CORYNEBACTERIUM. | 0 | 2.4 | 2 | 0 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 1.98 | 1 | 0 |
Pilonidal Cyst [description not available] | 0 | 4.5 | 3 | 0 |
Pilonidal Sinus A hair-containing cyst or sinus, occurring chiefly in the coccygeal region. | 0 | 4.5 | 3 | 0 |
Exfoliation Glaucoma [description not available] | 0 | 1.98 | 1 | 0 |
Exfoliation Syndrome The deposition of flaky, translucent fibrillar material most conspicuous on the anterior lens capsule and pupillary margin but also in both surfaces of the iris, the zonules, trabecular meshwork, ciliary body, corneal endothelium, and orbital blood vessels. It sometimes forms a membrane on the anterior iris surface. Exfoliation refers to the shedding of pigment by the iris. (Newell, Ophthalmology, 7th ed, p380) | 0 | 1.98 | 1 | 0 |
Christmas Disease [description not available] | 0 | 1.98 | 1 | 0 |
Hemophilia B A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) | 0 | 1.98 | 1 | 0 |
Bronchiolitis Inflammation of the BRONCHIOLES. | 0 | 2.39 | 2 | 0 |
Adolescent Gynecomastia [description not available] | 0 | 3.07 | 5 | 0 |
Gynecomastia Enlargement of the BREAST in the males, caused by an excess of ESTROGENS. Physiological gynecomastia is normally observed in NEWBORNS; ADOLESCENT; and AGING males. | 0 | 3.07 | 5 | 0 |
Arthritides, Bacterial [description not available] | 0 | 1.98 | 1 | 0 |
Mycoplasma dispar Infection [description not available] | 0 | 1.98 | 1 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 1.98 | 1 | 0 |
Ovarian Diseases Pathological processes of the OVARY. | 0 | 2.89 | 4 | 0 |
Cutaneous Fistula An abnormal passage or communication leading from an internal organ to the surface of the body. | 0 | 2.4 | 2 | 0 |
Ischemia A hypoperfusion of the BLOOD through an organ or tissue caused by a PATHOLOGIC CONSTRICTION or obstruction of its BLOOD VESSELS, or an absence of BLOOD CIRCULATION. | 0 | 3.09 | 5 | 0 |
Bile Duct Obstruction, Extrahepatic [description not available] | 0 | 2.9 | 4 | 0 |
Orthopedic Disorders [description not available] | 0 | 1.98 | 1 | 0 |
Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | 0 | 1.98 | 1 | 0 |
Acute Promyelocytic Leukemia [description not available] | 0 | 2.67 | 3 | 0 |
Leukemia, Promyelocytic, Acute An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 2.67 | 3 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 3.36 | 7 | 0 |
Cerebellar Diseases Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. | 0 | 2.38 | 2 | 0 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 3.07 | 5 | 0 |
Retinoblastoma A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104) | 0 | 3.07 | 5 | 0 |
Injuries, Multiple [description not available] | 0 | 2.39 | 2 | 0 |
Abrasion, Dental [description not available] | 0 | 1.98 | 1 | 0 |
Coronary Heart Disease [description not available] | 0 | 1.98 | 1 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 1.98 | 1 | 0 |
Arteriosclerosis Thickening and loss of elasticity of the walls of ARTERIES of all sizes. There are many forms classified by the types of lesions and arteries involved, such as ATHEROSCLEROSIS with fatty lesions in the ARTERIAL INTIMA of medium and large muscular arteries. | 0 | 3.48 | 8 | 0 |
Coronary Disease An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYOCARDIAL ISCHEMIA (insufficient blood supply to the heart muscle) caused by a decreased capacity of the coronary vessels. | 0 | 1.98 | 1 | 0 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 1.98 | 1 | 0 |
Periodontitis, Acute Nonsuppurative [description not available] | 0 | 2.38 | 2 | 0 |
Exposure, Dental Pulp [description not available] | 0 | 1.98 | 1 | 0 |
Dental Pulp Exposure The result of pathological changes in the hard tissue of a tooth caused by carious lesions, mechanical factors, or trauma, which render the pulp susceptible to bacterial invasion from the external environment. | 0 | 1.98 | 1 | 0 |
Periapical Periodontitis Inflammation of the PERIAPICAL TISSUE. It includes general, unspecified, or acute nonsuppurative inflammation. Chronic nonsuppurative inflammation is PERIAPICAL GRANULOMA. Suppurative inflammation is PERIAPICAL ABSCESS. | 0 | 2.38 | 2 | 0 |
Interstitial Nephritis [description not available] | 0 | 2.39 | 2 | 0 |
Nephritis, Interstitial Inflammation of the interstitial tissue of the kidney. This term is generally used for primary inflammation of KIDNEY TUBULES and/or surrounding interstitium. For primary inflammation of glomerular interstitium, see GLOMERULONEPHRITIS. Infiltration of the inflammatory cells into the interstitial compartment results in EDEMA, increased spaces between the tubules, and tubular renal dysfunction. | 0 | 2.39 | 2 | 0 |
Hepatitis, Animal INFLAMMATION of the LIVER in non-human animals. | 0 | 2.39 | 2 | 0 |
Xerophthalmia Dryness of the eye surfaces caused by deficiency of tears or conjunctival secretions. It may be associated with vitamin A deficiency, trauma, or any condition in which the eyelids do not close completely. | 0 | 2.36 | 2 | 0 |
Mushroom Poisoning Poisoning from ingestion of mushrooms, primarily from, but not restricted to, toxic varieties. | 0 | 1.98 | 1 | 0 |
Myofibromatosis A condition characterized by multiple formations of myofibromas (LEIOMYOMA). | 0 | 2.9 | 1 | 0 |
Bronchitis Inflammation of the large airways in the lung including any part of the BRONCHI, from the PRIMARY BRONCHI to the TERTIARY BRONCHI. | 0 | 2.39 | 2 | 0 |
Complication, Intraoperative [description not available] | 0 | 1.99 | 1 | 0 |
Bone Hypertrophy [description not available] | 0 | 1.98 | 1 | 0 |
Pigmentary Retinopathy [description not available] | 0 | 2.36 | 2 | 0 |
Retinitis Pigmentosa Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina. | 0 | 2.36 | 2 | 0 |
Adenoma, Villous An adenoma of the large intestine. It is usually a solitary, sessile, often large, tumor of colonic mucosa composed of mucinous epithelium covering delicate vascular projections. Hypersecretion and malignant changes occur frequently. (Stedman, 25th ed) | 0 | 3.31 | 2 | 0 |
Idiopathic Parkinson Disease [description not available] | 0 | 2.9 | 1 | 0 |
Parkinson Disease A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75) | 0 | 2.9 | 1 | 0 |
Paraneoplastic Syndromes In patients with neoplastic diseases a wide variety of clinical pictures which are indirect and usually remote effects produced by tumor cell metabolites or other products. | 0 | 2.68 | 3 | 0 |
Hay Fever [description not available] | 0 | 1.99 | 1 | 0 |
Rhinitis, Allergic, Seasonal Allergic rhinitis that occurs at the same time every year. It is characterized by acute CONJUNCTIVITIS with lacrimation and ITCHING, and regarded as an allergic condition triggered by specific ALLERGENS. | 0 | 1.99 | 1 | 0 |
Endarteritis Inflammation of the inner endothelial lining (TUNICA INTIMA) of an artery. | 0 | 1.99 | 1 | 0 |
Obstructive Lung Diseases [description not available] | 0 | 1.99 | 1 | 0 |
Lung Diseases, Obstructive Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent. | 0 | 1.99 | 1 | 0 |
Bronchial Diseases Diseases involving the BRONCHI. | 0 | 2.9 | 1 | 0 |
Rhinophyma A manifestation of severe ROSACEA resulting in significant enlargement of the NOSE and occurring primarily in men. It is caused by hypertrophy of the SEBACEOUS GLANDS and surrounding CONNECTIVE TISSUE. The nose is reddened and marked with TELANGIECTASIS. | 0 | 2.39 | 2 | 0 |
Transmissible Venereal Tumors [description not available] | 0 | 2.38 | 2 | 0 |
Blood Pressure, Low [description not available] | 0 | 1.99 | 1 | 0 |
Hypotension Abnormally low BLOOD PRESSURE that can result in inadequate blood flow to the brain and other vital organs. Common symptom is DIZZINESS but greater negative impacts on the body occur when there is prolonged depravation of oxygen and nutrients. | 0 | 1.99 | 1 | 0 |
Hakim Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
Hydrocephalus, Normal Pressure A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see GAIT DISORDERS, NEUROLOGIC), progressive intellectual decline, and URINARY INCONTINENCE. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of CSF including SUBARACHNOID HEMORRHAGE, chronic MENINGITIS, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3) | 0 | 1.98 | 1 | 0 |
Chromosomal Triplication [description not available] | 0 | 4.41 | 8 | 0 |
Injuries, Leg [description not available] | 0 | 2.37 | 2 | 0 |
Bladder Calculi [description not available] | 0 | 1.99 | 1 | 0 |
Balkan Endemic Nephropathy [description not available] | 0 | 1.99 | 1 | 0 |
Keratoconjunctivitis Simultaneous inflammation of the cornea and conjunctiva. | 0 | 3.06 | 5 | 0 |
Dementia Multi-Infarct [description not available] | 0 | 1.99 | 1 | 0 |
Congenital Poikiloderma [description not available] | 0 | 2.39 | 2 | 0 |
Adrenal Gland Hypofunction [description not available] | 0 | 1.99 | 1 | 0 |
Achalasia [description not available] | 0 | 2.4 | 2 | 0 |
Adrenal Insufficiency Conditions in which the production of adrenal CORTICOSTEROIDS falls below the requirement of the body. Adrenal insufficiency can be caused by defects in the ADRENAL GLANDS, the PITUITARY GLAND, or the HYPOTHALAMUS. | 0 | 1.99 | 1 | 0 |
Esophageal Achalasia A motility disorder of the ESOPHAGUS in which the LOWER ESOPHAGEAL SPHINCTER (near the CARDIA) fails to relax resulting in functional obstruction of the esophagus, and DYSPHAGIA. Achalasia is characterized by a grossly contorted and dilated esophagus (megaesophagus). | 0 | 2.4 | 2 | 0 |
Childhood Torsion Disease [description not available] | 0 | 2.9 | 1 | 0 |
22q11.2 Deletion Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
DiGeorge Syndrome Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies. | 0 | 1.99 | 1 | 0 |
Parotiditis [description not available] | 0 | 1.99 | 1 | 0 |
Haim-Monk Syndrome [description not available] | 0 | 2.67 | 3 | 0 |
Absence of Brain, Congenital [description not available] | 0 | 2.38 | 2 | 0 |
Adenoma, Prolactin-Secreting, Pituitary [description not available] | 0 | 1.99 | 1 | 0 |
Hidrocystoma A cystic form of sweat gland adenoma (ADENOMA, SWEAT GLAND). It is produced by the cystic proliferation of apocrine secretory glands. It is not uncommon, occurring in adult life in no particular age group, with males and females equally affected. The commonest site is around the eye, particularly lateral to the outer canthus. It is cured by surgical removal. (Stedman, 25th ed; Rook et al., Textbook of Dermatology, 4th ed, p2410) | 0 | 2.91 | 4 | 0 |
Cold Sore [description not available] | 0 | 2.38 | 2 | 0 |
Gingivostomatitis, Herpetic [description not available] | 0 | 1.99 | 1 | 0 |
Herpes Labialis Herpes simplex, caused by type 1 virus, primarily spread by oral secretions and usually occurring as a concomitant of fever. It may also develop in the absence of fever or prior illness. It commonly involves the facial region, especially the lips and the nares. (Dorland, 27th ed.) | 0 | 2.38 | 2 | 0 |
Stomatitis, Herpetic Stomatitis caused by Herpesvirus hominis. It usually occurs as acute herpetic stomatitis (or gingivostomatitis), an oral manifestation of primary herpes simplex seen primarily in children and adolescents. | 0 | 1.99 | 1 | 0 |
Venous Insufficiency Impaired venous blood flow or venous return (venous stasis), usually caused by inadequate venous valves. Venous insufficiency often occurs in the legs, and is associated with EDEMA and sometimes with VENOUS STASIS ULCERS at the ankle. | 0 | 2.38 | 2 | 0 |
Urethral Obstruction Partial or complete blockage in any part of the URETHRA that can lead to difficulty or inability to empty the URINARY BLADDER. It is characterized by an enlarged, often damaged, bladder with frequent urges to void. | 0 | 1.99 | 1 | 0 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 3.31 | 2 | 0 |
Chromosome Inversion An aberration in which a chromosomal segment is deleted and reinserted in the same place but turned 180 degrees from its original orientation, so that the gene sequence for the segment is reversed with respect to that of the rest of the chromosome. | 0 | 2.91 | 1 | 0 |
Hyperkyphosis [description not available] | 0 | 2.91 | 1 | 0 |
BCKD Deficiency [description not available] | 0 | 2.9 | 1 | 0 |
Maple Syrup Urine Disease An autosomal recessive inherited disorder with multiple forms of phenotypic expression, caused by a defect in the oxidative decarboxylation of branched-chain amino acids (AMINO ACIDS, BRANCHED-CHAIN). These metabolites accumulate in body fluids and render a maple syrup odor. The disease is divided into classic, intermediate, intermittent, and thiamine responsive subtypes. The classic form presents in the first week of life with ketoacidosis, hypoglycemia, emesis, neonatal seizures, and hypertonia. The intermediate and intermittent forms present in childhood or later with acute episodes of ataxia and vomiting. (From Adams et al., Principles of Neurology, 6th ed, p936) | 0 | 2.9 | 1 | 0 |
Ureteral Diseases Pathological processes involving the URETERS. | 0 | 1.99 | 1 | 0 |
Pancreatic Pseudocyst Cyst-like space not lined by EPITHELIUM and contained within the PANCREAS. Pancreatic pseudocysts account for most of the cystic collections in the pancreas and are often associated with chronic PANCREATITIS. | 0 | 1.99 | 1 | 0 |
Antidiuretic Hormone, Inappropriate Secretion [description not available] | 0 | 1.99 | 1 | 0 |
Inappropriate ADH Syndrome A condition of HYPONATREMIA and renal salt loss attributed to overexpansion of BODY FLUIDS resulting from sustained release of ANTIDIURETIC HORMONES which stimulates renal resorption of water. It is characterized by normal KIDNEY function, high urine OSMOLALITY, low serum osmolality, and neurological dysfunction. Etiologies include ADH-producing neoplasms, injuries or diseases involving the HYPOTHALAMUS, the PITUITARY GLAND, and the LUNG. This syndrome can also be drug-induced. | 0 | 1.99 | 1 | 0 |
Infections, Orthomyxoviridae [description not available] | 0 | 1.99 | 1 | 0 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 1.99 | 1 | 0 |
Leg Dermatoses A nonspecific term used to denote any cutaneous lesion or group of lesions, or eruptions of any type on the leg. (From Stedman, 25th ed) | 0 | 2.37 | 2 | 0 |
Inner Ear Disease [description not available] | 0 | 2.39 | 2 | 0 |
Otospongiosis [description not available] | 0 | 1.99 | 1 | 0 |
Labyrinth Diseases Pathological processes of the inner ear (LABYRINTH) which contains the essential apparatus of hearing (COCHLEA) and balance (SEMICIRCULAR CANALS). | 0 | 2.39 | 2 | 0 |
Otosclerosis Formation of spongy bone in the labyrinth capsule which can progress toward the STAPES (stapedial fixation) or anteriorly toward the COCHLEA leading to conductive, sensorineural, or mixed HEARING LOSS. Several genes are associated with familial otosclerosis with varied clinical signs. | 0 | 1.99 | 1 | 0 |
Anus Prolapse [description not available] | 0 | 1.99 | 1 | 0 |
Gonadal Agenesis The complete failure of gonadal development. | 0 | 1.99 | 1 | 0 |
Cerebral Pseudosclerosis [description not available] | 0 | 1.99 | 1 | 0 |
Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. | 0 | 1.99 | 1 | 0 |
Glomangioma [description not available] | 0 | 2.39 | 2 | 0 |
Hypomelanosis [description not available] | 0 | 1.99 | 1 | 0 |
Hypopigmentation A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections. | 0 | 1.99 | 1 | 0 |
Keratitis, Acanthamoeba [description not available] | 0 | 1.99 | 1 | 0 |
Acanthamoeba Keratitis Infection of the cornea by an ameboid protozoan which may cause corneal ulceration leading to blindness. | 0 | 1.99 | 1 | 0 |
Cardiac Failure [description not available] | 0 | 1.99 | 1 | 0 |
Angiitis [description not available] | 0 | 2.41 | 2 | 0 |
Heart Failure A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION. | 0 | 1.99 | 1 | 0 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 2.41 | 2 | 0 |
Exophthalmos Abnormal protrusion of both eyes; may be caused by endocrine gland malfunction, malignancy, injury, or paralysis of the extrinsic muscles of the eye. | 0 | 1.99 | 1 | 0 |
Antibiotic-Associated Colitis [description not available] | 0 | 1.99 | 1 | 0 |
Enterocolitis, Pseudomembranous An acute inflammation of the INTESTINAL MUCOSA that is characterized by the presence of pseudomembranes or plaques in the SMALL INTESTINE (pseudomembranous enteritis) and the LARGE INTESTINE (pseudomembranous colitis). It is commonly associated with antibiotic therapy and CLOSTRIDIUM DIFFICILE colonization. | 0 | 1.99 | 1 | 0 |
Acariasis [description not available] | 0 | 2.67 | 3 | 0 |
Parasitic Skin Diseases [description not available] | 0 | 1.99 | 1 | 0 |
Adverse Drug Event [description not available] | 0 | 2.91 | 1 | 0 |
Drug-Related Side Effects and Adverse Reactions Disorders that result from the intended use of PHARMACEUTICAL PREPARATIONS. Included in this heading are a broad variety of chemically-induced adverse conditions due to toxicity, DRUG INTERACTIONS, and metabolic effects of pharmaceuticals. | 0 | 2.91 | 1 | 0 |
Infections, Hepadnaviridae [description not available] | 0 | 1.99 | 1 | 0 |
Hepadnaviridae Infections Virus diseases caused by the HEPADNAVIRIDAE. | 0 | 1.99 | 1 | 0 |
Adnexitis Inflammation of the uterine appendages (ADNEXA UTERI) including infection of the FALLOPIAN TUBES (SALPINGITIS), the ovaries (OOPHORITIS), or the supporting ligaments (PARAMETRITIS). | 0 | 2.4 | 2 | 0 |
Pelvic Inflammatory Disease A spectrum of inflammation involving the female upper genital tract and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Infection may be confined to the uterus (ENDOMETRITIS), the FALLOPIAN TUBES; (SALPINGITIS); the ovaries (OOPHORITIS), the supporting ligaments (PARAMETRITIS), or may involve several of the above uterine appendages. Such inflammation can lead to functional impairment and infertility. | 0 | 2.4 | 2 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 2.68 | 3 | 0 |
Leukemia, Lymphocytic, Chronic, B-Cell A chronic leukemia characterized by abnormal B-lymphocytes and often generalized lymphadenopathy. In patients presenting predominately with blood and bone marrow involvement it is called chronic lymphocytic leukemia (CLL); in those predominately with enlarged lymph nodes it is called small lymphocytic lymphoma. These terms represent spectrums of the same disease. | 0 | 2.68 | 3 | 0 |
Gestational Pemphigoid [description not available] | 0 | 1.99 | 1 | 0 |
Albinism General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair. | 0 | 2.87 | 4 | 0 |
Lassitude [description not available] | 0 | 1.99 | 1 | 0 |
Anorexia The lack or loss of APPETITE accompanied by an aversion to food and the inability to eat. It is the defining characteristic of the disorder ANOREXIA NERVOSA. | 0 | 2.4 | 2 | 0 |
Fatigue The state of weariness following a period of exertion, mental or physical, characterized by a decreased capacity for work and reduced efficiency to respond to stimuli. | 0 | 1.99 | 1 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 1.99 | 1 | 0 |
Cardiac Diseases [description not available] | 0 | 3.32 | 2 | 0 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 3.32 | 2 | 0 |
Carotid Body Tumor Benign paraganglioma at the bifurcation of the COMMON CAROTID ARTERIES. It can encroach on the parapharyngeal space and produce dysphagia, pain, and cranial nerve palsies. | 0 | 1.99 | 1 | 0 |
Hypercoagulability [description not available] | 0 | 1.99 | 1 | 0 |
Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 1.99 | 1 | 0 |
Nevus, Epithelioid and Spindle Cell A benign compound nevus occurring most often in children before puberty, composed of spindle and epithelioid cells located mainly in the dermis, sometimes in association with large atypical cells and multinucleate cells, and having a close histopathological resemblance to malignant melanoma. The tumor presents as a smooth to slightly scaly, round to oval, raised, firm papule or nodule, ranging in color from pink-tan to purplish red, often with surface telangiectasia. (Dorland, 27th ed) | 0 | 2.41 | 2 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 1.99 | 1 | 0 |
Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | 0 | 1.99 | 1 | 0 |
Diabetic Nephropathies KIDNEY injuries associated with diabetes mellitus and affecting KIDNEY GLOMERULUS; ARTERIOLES; KIDNEY TUBULES; and the interstitium. Clinical signs include persistent PROTEINURIA, from microalbuminuria progressing to ALBUMINURIA of greater than 300 mg/24 h, leading to reduced GLOMERULAR FILTRATION RATE and END-STAGE RENAL DISEASE. | 0 | 1.99 | 1 | 0 |
Bronze Diabetes [description not available] | 0 | 2.67 | 3 | 0 |
Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) | 0 | 2.67 | 3 | 0 |
Tongue, Hairy A benign condition of the tongue characterized by hypertrophy of the filiform papillae that give the dorsum of the tongue a furry appearance. The color of the elongated papillae varies from yellowish white to brown or black, depending upon staining by substances such as tobacco, food, or drugs. (Dorland, 27th ed) | 0 | 2 | 1 | 0 |
Spider Veins [description not available] | 0 | 2.88 | 4 | 0 |
Telangiectasis Permanent dilation of preexisting blood vessels (CAPILLARIES; ARTERIOLES; VENULES) creating small focal red lesions, most commonly in the skin or mucous membranes. It is characterized by the prominence of skin blood vessels, such as vascular spiders. | 0 | 2.88 | 4 | 0 |
Constriction, Pathological [description not available] | 0 | 2.4 | 2 | 0 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 2.4 | 2 | 0 |
Pulmonary Sarcoidosis [description not available] | 0 | 2.39 | 2 | 0 |
Sarcoidosis, Pulmonary Sarcoidosis affecting predominantly the lungs, the site most frequently involved and most commonly causing morbidity and mortality in sarcoidosis. Pulmonary sarcoidosis is characterized by sharply circumscribed granulomas in the alveolar, bronchial, and vascular walls, composed of tightly packed cells derived from the mononuclear phagocyte system. The clinical symptoms when present are dyspnea upon exertion, nonproductive cough, and wheezing. (Cecil Textbook of Medicine, 19th ed, p431) | 0 | 2.39 | 2 | 0 |
Cyst, Lymphatic [description not available] | 0 | 2 | 1 | 0 |
Bacterial Conjunctivitides [description not available] | 0 | 2 | 1 | 0 |
Blepharitis Inflammation of the eyelids. | 0 | 2.68 | 3 | 0 |
Conjunctivitis, Bacterial Purulent infections of the conjunctiva by several species of gram-negative, gram-positive, or acid-fast organisms. Some of the more commonly found genera causing conjunctival infections are Haemophilus, Streptococcus, Neisseria, and Chlamydia. | 0 | 2 | 1 | 0 |
Atopic Hypersensitivity [description not available] | 0 | 4.26 | 4 | 0 |
Airway Hyper-Responsiveness [description not available] | 0 | 2.91 | 1 | 0 |
Diseases of Pharynx [description not available] | 0 | 2.91 | 1 | 0 |
Orbital Diseases Diseases of the bony orbit and contents except the eyeball. | 0 | 3.31 | 2 | 0 |
Choked Disk [description not available] | 0 | 2 | 1 | 0 |
Papilledema Swelling of the OPTIC DISK, usually in association with increased intracranial pressure, characterized by hyperemia, blurring of the disk margins, microhemorrhages, blind spot enlargement, and engorgement of retinal veins. Chronic papilledema may cause OPTIC ATROPHY and visual loss. (Miller et al., Clinical Neuro-Ophthalmology, 4th ed, p175) | 0 | 2 | 1 | 0 |
Panuveitis Inflammation in which both the anterior and posterior segments of the uvea are involved and a specific focus is not apparent. It is often severe and extensive and a serious threat to vision. Causes include systemic diseases such as tuberculosis, sarcoidosis, and syphilis, as well as malignancies. The intermediate segment of the eye is not involved. | 0 | 2 | 1 | 0 |
Keratitis, Ulcerative [description not available] | 0 | 2.37 | 2 | 0 |
Corneal Ulcer Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue; usually caused by bacterial, fungal, or viral infection. | 0 | 2.37 | 2 | 0 |
Branch Vein Occlusion [description not available] | 0 | 1.99 | 1 | 0 |
Retinal Vein Occlusion Blockage of the RETINAL VEIN. Those at high risk for this condition include patients with HYPERTENSION; DIABETES MELLITUS; ATHEROSCLEROSIS; and other CARDIOVASCULAR DISEASES. | 0 | 1.99 | 1 | 0 |
Foot Injuries General or unspecified injuries involving the foot. | 0 | 2 | 1 | 0 |
Intestinal Perforation Opening or penetration through the wall of the INTESTINES. | 0 | 2 | 1 | 0 |
Ileitis Inflammation of any segment of the ILEUM and the ILEOCECAL VALVE. | 0 | 2.39 | 2 | 0 |
Central Retinal Edema, Cystoid [description not available] | 0 | 2 | 1 | 0 |
Macular Edema Fluid accumulation in the outer layer of the MACULA LUTEA that results from intraocular or systemic insults. It may develop in a diffuse pattern where the macula appears thickened or it may acquire the characteristic petaloid appearance referred to as cystoid macular edema. Although macular edema may be associated with various underlying conditions, it is most commonly seen following intraocular surgery, venous occlusive disease, DIABETIC RETINOPATHY, and posterior segment inflammatory disease. (From Survey of Ophthalmology 2004; 49(5) 470-90) | 0 | 2 | 1 | 0 |
Chorioadenoma [description not available] | 0 | 2 | 1 | 0 |
Aseptic Meningitis [description not available] | 0 | 2 | 1 | 0 |
Meningitis, Aseptic A syndrome characterized by headache, neck stiffness, low grade fever, and CSF lymphocytic pleocytosis in the absence of an acute bacterial pathogen. Viral meningitis is the most frequent cause although MYCOPLASMA INFECTIONS; RICKETTSIA INFECTIONS; diagnostic or therapeutic procedures; NEOPLASTIC PROCESSES; septic perimeningeal foci; and other conditions may result in this syndrome. (From Adams et al., Principles of Neurology, 6th ed, p745) | 0 | 2 | 1 | 0 |
Blue Nevi [description not available] | 0 | 2 | 1 | 0 |
Complications, Hematologic Pregnancy [description not available] | 0 | 2 | 1 | 0 |
Deficiency, Factor 13 [description not available] | 0 | 2 | 1 | 0 |
Factor XIII Deficiency A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis. | 0 | 2 | 1 | 0 |
Leukemic Infiltration A pathologic change in leukemia in which leukemic cells permeate various organs at any stage of the disease. All types of leukemia show various degrees of infiltration, depending upon the type of leukemia. The degree of infiltration may vary from site to site. The liver and spleen are common sites of infiltration, the greatest appearing in myelocytic leukemia, but infiltration is seen also in the granulocytic and lymphocytic types. The kidney is also a common site and of the gastrointestinal system, the stomach and ileum are commonly involved. In lymphocytic leukemia the skin is often infiltrated. The central nervous system too is a common site. | 0 | 2 | 1 | 0 |
Adult Spinal Muscular Atrophy [description not available] | 0 | 1.99 | 1 | 0 |
Muscular Atrophy, Spinal A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 1.99 | 1 | 0 |
Plant Poisoning Poisoning by the ingestion of plants or its leaves, berries, roots or stalks. The manifestations in both humans and animals vary in severity from mild to life threatening. In animals, especially domestic animals, it is usually the result of ingesting moldy or fermented forage. | 0 | 2 | 1 | 0 |
P carinii Pneumonia [description not available] | 0 | 2 | 1 | 0 |
Neutropenia A decrease in the number of NEUTROPHILS found in the blood. | 0 | 2 | 1 | 0 |
Pneumonia, Pneumocystis A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis. | 0 | 2 | 1 | 0 |
Human T-lymphotropic Virus 1 Infection [description not available] | 0 | 2 | 1 | 0 |
HTLV-I Infections Diseases caused by HUMAN T-LYMPHOTROPIC VIRUS 1. | 0 | 2 | 1 | 0 |
Melena The black, tarry, foul-smelling FECES that contain degraded blood. | 0 | 2 | 1 | 0 |
Circulatory Collapse [description not available] | 0 | 2 | 1 | 0 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 2 | 1 | 0 |
B cepacia Infection [description not available] | 0 | 2 | 1 | 0 |
Chondrodystrophic Myotonia [description not available] | 0 | 2 | 1 | 0 |
Urethritis Inflammation involving the URETHRA. Similar to CYSTITIS, clinical symptoms range from vague discomfort to painful urination (DYSURIA), urethral discharge, or both. | 0 | 2 | 1 | 0 |
Fibrous Dysplasia, Monostotic FIBROUS DYSPLASIA OF BONE involving only one bone. | 0 | 2 | 1 | 0 |
Eosinophilia, Pulmonary [description not available] | 0 | 2 | 1 | 0 |
Pulmonary Eosinophilia A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents. | 0 | 2 | 1 | 0 |
Ankylosis Fixation and immobility of a joint. | 0 | 2 | 1 | 0 |
Atresia, Esophageal [description not available] | 0 | 2 | 1 | 0 |
Esophageal Atresia Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA. | 0 | 2 | 1 | 0 |
Clonorchiasis Infection of the biliary passages with CLONORCHIS SINENSIS, also called Opisthorchis sinensis. It may lead to inflammation of the biliary tract, proliferation of biliary epithelium, progressive portal fibrosis, and sometimes bile duct carcinoma. Extension to the liver may lead to fatty changes and cirrhosis. (From Dorland, 27th ed) | 0 | 2 | 1 | 0 |
Atelectasis [description not available] | 0 | 2.92 | 1 | 0 |
Atherosclerotic Parkinsonism [description not available] | 0 | 2.92 | 1 | 0 |
Parkinson Disease, Secondary Conditions which feature clinical manifestations resembling primary Parkinson disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42) | 0 | 2.92 | 1 | 0 |
Urinary Calculi Low-density crystals or stones in any part of the URINARY TRACT. Their chemical compositions often include CALCIUM OXALATE, magnesium ammonium phosphate (struvite), CYSTINE, or URIC ACID. | 0 | 2 | 1 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 2 | 1 | 0 |
Ischemic Attack, Transient Brief reversible episodes of focal, nonconvulsive ischemic dysfunction of the brain having a duration of less than 24 hours, and usually less than one hour, caused by transient thrombotic or embolic blood vessel occlusion or stenosis. Events may be classified by arterial distribution, temporal pattern, or etiology (e.g., embolic vs. thrombotic). (From Adams et al., Principles of Neurology, 6th ed, pp814-6) | 0 | 2 | 1 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 2 | 1 | 0 |
Arteriosclerosis, Coronary [description not available] | 0 | 2 | 1 | 0 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 2 | 1 | 0 |
Infection [description not available] | 0 | 3.58 | 3 | 0 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 3.58 | 3 | 0 |
Animal Diseases Diseases that occur in VERTEBRATE animals. | 0 | 2 | 1 | 0 |
Caroli Disease Congenital cystic dilatation of the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). It consists of 2 types: simple Caroli disease is characterized by bile duct dilatation (ectasia) alone; and complex Caroli disease is characterized by bile duct dilatation with extensive hepatic fibrosis and portal hypertension (HYPERTENSION, PORTAL). Benign renal tubular ectasia is associated with both types of Caroli disease. | 0 | 2 | 1 | 0 |
Angiofibroma A benign neoplasm of fibrous tissue in which there are numerous small and large, frequently dilated, vascular channels. (Stedman, 25th ed) | 0 | 2.92 | 1 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 2.92 | 1 | 0 |
Hemorrhage, Peptic Ulcer [description not available] | 0 | 2.92 | 1 | 0 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 2.92 | 1 | 0 |
Infectious Endophthalmitis Infectious condition of the internal eye. | 0 | 2 | 1 | 0 |
Endophthalmitis Suppurative inflammation of the tissues of the internal structures of the eye frequently associated with an infection. | 0 | 2 | 1 | 0 |
Rhabdomyoma A benign tumor derived from striated muscle. It is extremely rare, generally occurring in the tongue, neck muscles, larynx, uvula, nasal cavity, axilla, vulva, and heart. These tumors are treated by simple excision. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1354) | 0 | 3.08 | 5 | 0 |
Angiomatosis Retinae [description not available] | 0 | 2.9 | 4 | 0 |
von Hippel-Lindau Disease An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. | 0 | 2.9 | 4 | 0 |
Hemorrhoids Swollen veins in the lower part of the RECTUM or ANUS. Hemorrhoids can be inside the anus (internal), under the skin around the anus (external), or protruding from inside to outside of the anus. People with hemorrhoids may or may not exhibit symptoms which include bleeding, itching, and pain. | 0 | 2.66 | 3 | 0 |
Rida [description not available] | 0 | 2 | 1 | 0 |
Leukemia, Smoldering [description not available] | 0 | 2 | 1 | 0 |
Anemia, Refractory, with Excess of Blasts Chronic refractory anemia with granulocytopenia, and/or thrombocytopenia. Myeloblasts and progranulocytes constitute 5 to 40 percent of the nucleated marrow cells. | 0 | 2 | 1 | 0 |
Alveolar Proteinoses, Pulmonary [description not available] | 0 | 2 | 1 | 0 |
Pulmonary Alveolar Proteinosis A PULMONARY ALVEOLI-filling disease, characterized by dense phospholipoproteinaceous deposits in the alveoli, cough, and DYSPNEA. This disease is often related to, congenital or acquired, impaired processing of PULMONARY SURFACTANTS by alveolar macrophages, a process dependent on GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR. | 0 | 2 | 1 | 0 |
Empyema, Pleural, Tuberculous [description not available] | 0 | 2 | 1 | 0 |
Hyperplasia, Reactive Lymphoid [description not available] | 0 | 2 | 1 | 0 |
Vestibular Diseases Pathological processes of the VESTIBULAR LABYRINTH which contains part of the balancing apparatus. Patients with vestibular diseases show instability and are at risk of frequent falls. | 0 | 2 | 1 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 2.41 | 2 | 0 |
Hypopituitarism Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions. | 0 | 2.41 | 2 | 0 |
Ductal, Lobular, and Medullary Neoplasms [description not available] | 0 | 2 | 1 | 0 |
Focal Nodular Hyperplasia Solitary or multiple benign hepatic vascular tumors, usually occurring in women of 20-50 years of age. The nodule, poorly encapsulated, consists of a central stellate fibrous scar and normal liver elements such as HEPATOCYTES, small BILE DUCTS, and KUPFFER CELLS among the intervening fibrous septa. The pale colored central scar represents large blood vessels with hyperplastic fibromuscular layer and narrowing lumen. | 0 | 2.41 | 2 | 0 |
Forestier-Certonciny Syndrome [description not available] | 0 | 2.39 | 2 | 0 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 2.39 | 2 | 0 |
Polymyalgia Rheumatica A syndrome in the elderly characterized by proximal joint and muscle pain, high erythrocyte sedimentation rate, and a self-limiting course. Pain is usually accompanied by evidence of an inflammatory reaction. Women are affected twice as commonly as men and Caucasians more frequently than other groups. The condition is frequently associated with GIANT CELL ARTERITIS and some theories pose the possibility that the two diseases arise from a single etiology or even that they are the same entity. | 0 | 2.39 | 2 | 0 |
Giant Cell Arteritis A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmural infiltrate containing multinucleated GIANT CELLS. The TEMPORAL ARTERY is commonly involved. This disorder appears primarily in people over the age of 50. Symptoms include FEVER; FATIGUE; HEADACHE; visual impairment; pain in the jaw and tongue; and aggravation of pain by cold temperatures. (From Adams et al., Principles of Neurology, 6th ed) | 0 | 2.39 | 2 | 0 |
Infections, Salmonella [description not available] | 0 | 2.41 | 2 | 0 |
Pleurisy, Tuberculous [description not available] | 0 | 2.01 | 1 | 0 |
Human Adenovirus Infections [description not available] | 0 | 2.01 | 1 | 0 |
Adenovirus Infections, Human Respiratory and conjunctival infections caused by 33 identified serotypes of human adenoviruses. | 0 | 2.01 | 1 | 0 |
Cardiovascular Pregnancy Complications [description not available] | 0 | 2 | 1 | 0 |
Ectromelia, Infectious A viral infection of mice, causing edema and necrosis followed by limb loss. | 0 | 2.01 | 1 | 0 |
Joint Pain [description not available] | 0 | 2.01 | 1 | 0 |
Arthralgia Pain in the joint. | 0 | 2.01 | 1 | 0 |
HbS Disease [description not available] | 0 | 2.87 | 1 | 0 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 2.87 | 1 | 0 |
Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. | 0 | 2.87 | 1 | 0 |
Buschke's Scleredema [description not available] | 0 | 2.35 | 2 | 0 |
Scleredema Adultorum A diffuse, non-pitting induration of the skin of unknown etiology that occurs most commonly in association with diabetes mellitus, predominantly in females. It typically begins on the face or head and spreads to other areas of the body, sometimes involving noncutaneous tissues. Often it is preceded by any of various infections, notably staphylococcal infections. The condition resolves spontaneously, usually within two years of onset. (From Dorland, 27th ed) | 0 | 2.35 | 2 | 0 |
alpha-Galactosidase A Deficiency [description not available] | 0 | 4.25 | 4 | 0 |
Chediak-Higashi Syndrome A form of phagocyte bactericidal dysfunction characterized by unusual oculocutaneous albinism, high incidence of lymphoreticular neoplasms, and recurrent pyogenic infections. In many cell types, abnormal lysosomes are present leading to defective pigment distribution and abnormal neutrophil functions. The disease is transmitted by autosomal recessive inheritance and a similar disorder occurs in the beige mouse, the Aleutian mink, and albino Hereford cattle. | 0 | 4.03 | 3 | 0 |
Fabry Disease An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. | 0 | 4.25 | 4 | 0 |
Parotid Duct Calculi [description not available] | 0 | 1.95 | 1 | 0 |
Dental Occlusion, Traumatic An occlusion resulting in overstrain and injury to teeth, periodontal tissue, or other oral structures. | 0 | 1.95 | 1 | 0 |
Alactasia [description not available] | 0 | 1.95 | 1 | 0 |
Lactose Intolerance The condition resulting from the absence or deficiency of LACTASE in the MUCOSA cells of the GASTROINTESTINAL TRACT, and the inability to break down LACTOSE in milk for ABSORPTION. Bacterial fermentation of the unabsorbed lactose leads to symptoms that range from a mild indigestion (DYSPEPSIA) to severe DIARRHEA. Lactose intolerance may be an inborn error or acquired. | 0 | 1.95 | 1 | 0 |
CBS Deficiency [description not available] | 0 | 3.55 | 3 | 0 |
Homocystinuria Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979) | 0 | 3.55 | 3 | 0 |
Hypocalcemia Reduction of the blood calcium below normal. Manifestations include hyperactive deep tendon reflexes, Chvostek's sign, muscle and abdominal cramps, and carpopedal spasm. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Dental Fistula An abnormal passage in the oral cavity on the gingiva. | 0 | 2.37 | 2 | 0 |
Dental Fluoroses [description not available] | 0 | 1.95 | 1 | 0 |
Fluorosis, Dental A chronic endemic form of hypoplasia of the dental enamel caused by drinking water with a high fluorine content during the time of tooth formation, and characterized by defective calcification that gives a white chalky appearance to the enamel, which gradually undergoes brown discoloration. (Jablonski's Dictionary of Dentistry, 1992, p286) | 0 | 1.95 | 1 | 0 |
Newcastle Disease An acute febrile, contagious, viral disease of birds caused by an AVULAVIRUS called NEWCASTLE DISEASE VIRUS. It is characterized by respiratory and nervous symptoms in fowl and is transmissible to man causing a severe, but transient conjunctivitis. | 0 | 2.35 | 2 | 0 |
Stunted Growth [description not available] | 0 | 2.64 | 3 | 0 |
Coxsackie Virus Infections [description not available] | 0 | 1.95 | 1 | 0 |
Growth Disorders Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth. | 0 | 2.64 | 3 | 0 |
Kraurosis Vulvae [description not available] | 0 | 1.95 | 1 | 0 |
Vulvar Lichen Sclerosus Atrophy and shriveling of the SKIN of the VULVA that is characterized by the whitish LICHEN SCLEROSUS appearance, inflammation, and PRURITUS. | 0 | 1.95 | 1 | 0 |
Focal Infection An infection at a specific location that may spread to another region of the body. | 0 | 1.98 | 1 | 0 |
Cane-Cutter Fever [description not available] | 0 | 1.98 | 1 | 0 |
Leptospirosis Infections with bacteria of the genus LEPTOSPIRA. | 0 | 1.98 | 1 | 0 |
Cranial Nerve II Diseases [description not available] | 0 | 1.98 | 1 | 0 |
Optic Nerve Diseases Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect. | 0 | 1.98 | 1 | 0 |
Nephrosclerosis Hardening of the KIDNEY due to infiltration by fibrous connective tissue (FIBROSIS), usually caused by renovascular diseases or chronic HYPERTENSION. Nephrosclerosis leads to renal ISCHEMIA. | 0 | 1.98 | 1 | 0 |
Cacosmia [description not available] | 0 | 2.38 | 2 | 0 |
Osteoma A benign tumor composed of bone tissue or a hard tumor of bonelike structure developing on a bone (homoplastic osteoma) or on other structures (heteroplastic osteoma). (From Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Congenital Limb Deformities [description not available] | 0 | 1.98 | 1 | 0 |
Osteopoikilosis An asymptomatic, autosomal dominant trait in which pea-sized sclerotic spots, prominent in the metaphyseal area, are accompanied by unique cutaneous lesions. These are yellowish papules or plaques with increased elastin content. (From Cecil Textbook of Medicine, 19th ed, pp1434-35) | 0 | 2.89 | 1 | 0 |
Aspiration, Meconium [description not available] | 0 | 1.98 | 1 | 0 |
Meconium Aspiration Syndrome A condition caused by inhalation of MECONIUM into the LUNG of FETUS or NEWBORN, usually due to vigorous respiratory movements during difficult PARTURITION or respiratory system abnormalities. Meconium aspirate may block small airways leading to difficulties in PULMONARY GAS EXCHANGE and ASPIRATION PNEUMONIA. | 0 | 1.98 | 1 | 0 |
Malassezia furfur Infection [description not available] | 0 | 1.98 | 1 | 0 |
Tinea Versicolor A common chronic, noninflammatory and usually symptomless disorder, characterized by the occurrence of multiple macular patches of all sizes and shapes, and varying in pigmentation from fawn-colored to brown. It is seen most frequently in hot, humid, tropical regions and is mostly caused by MALASSEZIA FURFUR (formerly Pityrosporum orbiculare). | 0 | 1.98 | 1 | 0 |
Diseases of Endocrine System [description not available] | 0 | 4.05 | 3 | 0 |
Adult Rickets [description not available] | 0 | 3.28 | 2 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 4.05 | 3 | 0 |
Osteomalacia Disorder caused by an interruption of the mineralization of organic bone matrix leading to bone softening, bone pain, and weakness. It is the adult form of rickets resulting from disruption of VITAMIN D; PHOSPHORUS; or CALCIUM homeostasis. | 0 | 3.28 | 2 | 0 |
Cachexia General ill health, malnutrition, and weight loss, usually associated with chronic disease. | 0 | 1.98 | 1 | 0 |
Infections, Nematomorpha [description not available] | 0 | 1.98 | 1 | 0 |
Helminthiasis, Animal Infestation of animals with parasitic worms of the helminth class. The infestation may be experimental or veterinary. | 0 | 1.98 | 1 | 0 |
Helminthiasis Infestation with parasitic worms of the helminth class. | 0 | 1.98 | 1 | 0 |
Renal Artery Stenosis [description not available] | 0 | 1.98 | 1 | 0 |
Renal Artery Obstruction Narrowing or occlusion of the RENAL ARTERY or arteries. It is due usually to ATHEROSCLEROSIS; FIBROMUSCULAR DYSPLASIA; THROMBOSIS; EMBOLISM, or external pressure. The reduced renal perfusion can lead to renovascular hypertension (HYPERTENSION, RENOVASCULAR). | 0 | 1.98 | 1 | 0 |
Inhalation Injury, Smoke [description not available] | 0 | 1.98 | 1 | 0 |
Sclerosis, Systemic [description not available] | 0 | 3.3 | 2 | 0 |
Scleroderma, Systemic A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA. | 0 | 3.3 | 2 | 0 |
Alagille Syndrome 1 [description not available] | 0 | 1.98 | 1 | 0 |
Alagille Syndrome A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC), and malformations in the cardiovascular system, the eyes, the vertebral column, and the facies. Major clinical features include JAUNDICE, and congenital heart disease with peripheral PULMONARY STENOSIS. Alagille syndrome may result from heterogeneous gene mutations, including mutations in JAG1 on CHROMOSOME 20 (Type 1) and NOTCH2 on CHROMOSOME 1 (Type 2). | 0 | 1.98 | 1 | 0 |
Dental Deposit [description not available] | 0 | 1.98 | 1 | 0 |
Catarrh Inflammation of a mucous membrane with increased flow of mucous in humans or animals. Catarrh is used mostly in a historical context. | 0 | 1.97 | 1 | 0 |
Craniocerebral Injuries [description not available] | 0 | 1.97 | 1 | 0 |
Atresia, Choanal [description not available] | 0 | 1.97 | 1 | 0 |
Common Cold A catarrhal disorder of the upper respiratory tract, which may be viral or a mixed infection. It generally involves a runny nose, nasal congestion, and sneezing. | 0 | 1.97 | 1 | 0 |
Craniocerebral Trauma Traumatic injuries involving the cranium and intracranial structures (i.e., BRAIN; CRANIAL NERVES; MENINGES; and other structures). Injuries may be classified by whether or not the skull is penetrated (i.e., penetrating vs. nonpenetrating) or whether there is an associated hemorrhage. | 0 | 1.97 | 1 | 0 |
Dacryoadenitis [description not available] | 0 | 1.97 | 1 | 0 |
Addison's Anemia [description not available] | 0 | 1.97 | 1 | 0 |
Di Guglielmo Disease [description not available] | 0 | 1.97 | 1 | 0 |
Leukemia, Erythroblastic, Acute A myeloproliferative disorder characterized by neoplastic proliferation of erythroblastic and myeloblastic elements with atypical erythroblasts and myeloblasts in the peripheral blood. | 0 | 1.97 | 1 | 0 |
Chronic Primary Open Angle Glaucoma [description not available] | 0 | 1.97 | 1 | 0 |
Glaucoma, Open-Angle Glaucoma in which the angle of the anterior chamber is open and the trabecular meshwork does not encroach on the base of the iris. | 0 | 1.97 | 1 | 0 |
Destombes-Rosai-Dorfman Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Histiocytosis, Sinus Benign, non-Langerhans-cell, histiocytic proliferative disorder that primarily affects the lymph nodes. It is often referred to as sinus histiocytosis with massive lymphadenopathy. | 0 | 1.97 | 1 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 1.97 | 1 | 0 |
Ritter Disease [description not available] | 0 | 1.97 | 1 | 0 |
Central Nervous System Origin Vertigo [description not available] | 0 | 1.97 | 1 | 0 |
Vertigo An illusion of movement, either of the external world revolving around the individual or of the individual revolving in space. Vertigo may be associated with disorders of the inner ear (EAR, INNER); VESTIBULAR NERVE; BRAINSTEM; or CEREBRAL CORTEX. Lesions in the TEMPORAL LOBE and PARIETAL LOBE may be associated with FOCAL SEIZURES that may feature vertigo as an ictal manifestation. (From Adams et al., Principles of Neurology, 6th ed, pp300-1) | 0 | 1.97 | 1 | 0 |
Ichthyosis, Sex-Linked [description not available] | 0 | 1.97 | 1 | 0 |
Actinomycetales Infections Infections with bacteria of the order ACTINOMYCETALES. | 0 | 1.97 | 1 | 0 |
Acoustic Trauma Usually refer to hearing loss due to a single noise event such as an explosion or shotgun blast. | 0 | 1.97 | 1 | 0 |
Hearing Loss, Noise-Induced Hearing loss due to exposure to explosive loud noise or chronic exposure to sound level greater than 85 dB. The hearing loss is often in the frequency range 4000-6000 hertz. | 0 | 1.97 | 1 | 0 |
Schistosoma haematobia Infection [description not available] | 0 | 3.22 | 6 | 0 |
Schistosomiasis haematobia A human disease caused by the infection of parasitic worms SCHISTOSOMA HAEMATOBIUM. It is endemic in AFRICA and parts of the MIDDLE EAST. Tissue damages most often occur in the URINARY TRACT, specifically the URINARY BLADDER. | 0 | 3.22 | 6 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 3.8 | 4 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 3.8 | 4 | 0 |
Vulvar Diseases Pathological processes of the VULVA. | 0 | 2.89 | 1 | 0 |
Carcinoma, Ehrlich Tumor A transplantable, poorly differentiated malignant tumor which appeared originally as a spontaneous breast carcinoma in a mouse. It grows in both solid and ascitic forms. | 0 | 1.97 | 1 | 0 |
Chromoblastomycosis Scaly papule or warty growth, caused by five fungi, that spreads as a result of satellite lesions affecting the foot or leg. The extremity may become swollen and, at its distal portion, covered with various nodular, tumorous, verrucous lesions that resemble cauliflower. In rare instances, the disease may begin on the hand or wrist and involve the entire upper extremity. (Arnold, Odom, and James, Andrew's Diseases of the Skin, 8th ed, p362) | 0 | 1.97 | 1 | 0 |
Adjustment Disorder [description not available] | 0 | 1.97 | 1 | 0 |
Akinetic-Rigid Variant of Huntington Disease [description not available] | 0 | 1.97 | 1 | 0 |
Adjustment Disorders Maladaptive reactions to identifiable psychosocial stressors occurring within a short time after onset of the stressor. They are manifested by either impairment in social or occupational functioning or by symptoms (depression, anxiety, etc.) that are in excess of a normal and expected reaction to the stressor. | 0 | 1.97 | 1 | 0 |
Huntington Disease A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4) | 0 | 1.97 | 1 | 0 |
Deficiency Diseases A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 2.87 | 4 | 0 |
Arterial Obstructive Diseases [description not available] | 0 | 1.97 | 1 | 0 |
Arterial Occlusive Diseases Pathological processes which result in the partial or complete obstruction of ARTERIES. They are characterized by greatly reduced or absence of blood flow through these vessels. They are also known as arterial insufficiency. | 0 | 1.97 | 1 | 0 |
Cold Fingers, Hereditary [description not available] | 0 | 1.96 | 1 | 0 |
Rheumatoid Nodule Subcutaneous nodules seen in 20-30% of rheumatoid arthritis patients. They may arise anywhere on the body, but are most frequently found over the bony prominences. The nodules are characterized histologically by dense areas of fibrinoid necrosis with basophilic streaks and granules, surrounded by a palisade of cells, mainly fibroblasts and histiocytes. | 0 | 1.96 | 1 | 0 |
Raynaud Disease An idiopathic vascular disorder characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or CYANOSIS in response to cold exposure or stress. | 0 | 1.96 | 1 | 0 |
Anemia, Hypoplastic [description not available] | 0 | 3.58 | 3 | 0 |
Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | 0 | 3.58 | 3 | 0 |
Anophthalmia [description not available] | 0 | 1.96 | 1 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 2.36 | 2 | 0 |
Borrelia Infections Infections with bacteria of the genus BORRELIA. | 0 | 1.96 | 1 | 0 |
Lung Diseases, Parasitic Infections of the lungs with parasites, most commonly by parasitic worms (HELMINTHS). | 0 | 2.88 | 1 | 0 |
Periphlebitis Periphlebitis is inflammation of the outer coat of a vein or of tissues surrounding the vein. | 0 | 1.96 | 1 | 0 |
Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). | 0 | 1.96 | 1 | 0 |
Amyoplasia Congenita [description not available] | 0 | 1.96 | 1 | 0 |
Acoustic Neuroma [description not available] | 0 | 1.96 | 1 | 0 |
Candidiasis, Cutaneous Candidiasis of the skin manifested as eczema-like lesions of the interdigital spaces, perleche, or chronic paronychia. (Dorland, 27th ed) | 0 | 1.96 | 1 | 0 |
Hansen Disease [description not available] | 0 | 3.22 | 6 | 0 |
Leprosy A chronic granulomatous infection caused by MYCOBACTERIUM LEPRAE. The granulomatous lesions are manifested in the skin, the mucous membranes, and the peripheral nerves. Two polar or principal types are lepromatous and tuberculoid. | 0 | 3.22 | 6 | 0 |
Hepatic Veno Occlusive Disease [description not available] | 0 | 1.97 | 1 | 0 |
Hepatic Veno-Occlusive Disease Liver disease that is caused by injuries to the ENDOTHELIAL CELLS of the vessels and subendothelial EDEMA, but not by THROMBOSIS. Extracellular matrix, rich in FIBRONECTINS, is usually deposited around the HEPATIC VEINS leading to venous outflow occlusion and sinusoidal obstruction. | 0 | 1.97 | 1 | 0 |
Histiocytic Sarcoma Malignant neoplasms composed of MACROPHAGES or DENDRITIC CELLS. Most histiocytic sarcomas present as localized tumor masses without a leukemic phase. Though the biological behavior of these neoplasms resemble lymphomas, their cell lineage is histiocytic not lymphoid. | 0 | 1.97 | 1 | 0 |
Leishmania Infection [description not available] | 0 | 1.97 | 1 | 0 |
Leishmaniasis A disease caused by any of a number of species of protozoa in the genus LEISHMANIA. There are four major clinical types of this infection: cutaneous (Old and New World) (LEISHMANIASIS, CUTANEOUS), diffuse cutaneous (LEISHMANIASIS, DIFFUSE CUTANEOUS), mucocutaneous (LEISHMANIASIS, MUCOCUTANEOUS), and visceral (LEISHMANIASIS, VISCERAL). | 0 | 1.97 | 1 | 0 |
Goldblatt Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Acute Kidney Tubular Necrosis [description not available] | 0 | 1.97 | 1 | 0 |
Hypertension, Renovascular Hypertension due to RENAL ARTERY OBSTRUCTION or compression. | 0 | 1.97 | 1 | 0 |
Kidney Tubular Necrosis, Acute Acute kidney failure resulting from destruction of EPITHELIAL CELLS of the KIDNEY TUBULES. It is commonly attributed to exposure to toxic agents or renal ISCHEMIA following severe TRAUMA. | 0 | 1.97 | 1 | 0 |
ARC [description not available] | 0 | 1.97 | 1 | 0 |
AIDS-Related Complex A prodromal phase of infection with the human immunodeficiency virus (HIV). Laboratory criteria separating AIDS-related complex (ARC) from AIDS include elevated or hyperactive B-cell humoral immune responses, compared to depressed or normal antibody reactivity in AIDS; follicular or mixed hyperplasia in ARC lymph nodes, leading to lymphocyte degeneration and depletion more typical of AIDS; evolving succession of histopathological lesions such as localization of Kaposi's sarcoma, signaling the transition to the full-blown AIDS. | 0 | 1.97 | 1 | 0 |
Cervicitis [description not available] | 0 | 1.97 | 1 | 0 |
Uterine Cervicitis Inflammation of the UTERINE CERVIX. | 0 | 1.97 | 1 | 0 |
Mast-Cell Sarcoma A unifocal malignant tumor that consists of atypical pathological MAST CELLS without systemic involvement. It causes local destructive growth in organs other than in skin or bone marrow. | 0 | 2.65 | 3 | 0 |
Pancytopenia Deficiency of all three cell elements of the blood, erythrocytes, leukocytes and platelets. | 0 | 2.88 | 1 | 0 |
MS (Multiple Sclerosis) [description not available] | 0 | 2.36 | 2 | 0 |
Multiple Sclerosis An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903) | 0 | 2.36 | 2 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 1.97 | 1 | 0 |
Pituitary Diseases Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures. | 0 | 1.97 | 1 | 0 |
Lupus Erythematosus, Cutaneous, Subacute [description not available] | 0 | 2.37 | 2 | 0 |
Lupus Erythematosus, Cutaneous A form of lupus erythematosus in which the skin may be the only organ involved or in which skin involvement precedes the spread into other body systems. It has been classified into three forms - acute (= LUPUS ERYTHEMATOSUS, SYSTEMIC with skin lesions), subacute, and chronic (= LUPUS ERYTHEMATOSUS, DISCOID). | 0 | 2.37 | 2 | 0 |
Ophthalmoplegia, Progressive Supranuclear [description not available] | 0 | 1.97 | 1 | 0 |
Supranuclear Palsy, Progressive A degenerative disease of the central nervous system characterized by balance difficulties; OCULAR MOTILITY DISORDERS (supranuclear ophthalmoplegia); DYSARTHRIA; swallowing difficulties; and axial DYSTONIA. Onset is usually in the fifth decade and disease progression occurs over several years. Pathologic findings include neurofibrillary degeneration and neuronal loss in the dorsal MESENCEPHALON; SUBTHALAMIC NUCLEUS; RED NUCLEUS; pallidum; dentate nucleus; and vestibular nuclei. (From Adams et al., Principles of Neurology, 6th ed, pp1076-7) | 0 | 1.97 | 1 | 0 |
Pediculosis [description not available] | 0 | 2.65 | 3 | 0 |
Lice Infestations Parasitic attack or subsistence on the skin by members of the order Phthiraptera, especially on humans by Pediculus humanus of the family Pediculidae. The hair of the head, eyelashes, and pubis is a frequent site of infestation. (From Dorland, 28th ed; Stedman, 26th ed) | 0 | 2.65 | 3 | 0 |
Duhring Disease [description not available] | 0 | 2.36 | 2 | 0 |
Dermatitis Herpetiformis Rare, chronic, papulo-vesicular disease characterized by an intensely pruritic eruption consisting of various combinations of symmetrical, erythematous, papular, vesicular, or bullous lesions. The disease is strongly associated with the presence of HLA-B8 and HLA-DR3 antigens. A variety of different autoantibodies has been detected in small numbers in patients with dermatitis herpetiformis. | 0 | 2.36 | 2 | 0 |
Ataxia Telangiectasia Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Ataxia Telangiectasia An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23). | 0 | 1.97 | 1 | 0 |
Schistosoma mansoni Infection [description not available] | 0 | 1.97 | 1 | 0 |
Schistosomiasis mansoni Schistosomiasis caused by Schistosoma mansoni. It is endemic in Africa, the Middle East, South America, and the Caribbean and affects mainly the bowel, spleen, and liver. | 0 | 1.97 | 1 | 0 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 1.97 | 1 | 0 |
Transfusion Reaction Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility. | 0 | 1.97 | 1 | 0 |
Maculopapular Cutaneous Mastocytosis [description not available] | 0 | 2.36 | 2 | 0 |
Amazon Black Fever [description not available] | 0 | 1.97 | 1 | 0 |
Hepatitis D INFLAMMATION of the LIVER in humans caused by HEPATITIS DELTA VIRUS, a defective RNA virus that can only infect HEPATITIS B patients. For its viral coating, hepatitis delta virus requires the HEPATITIS B SURFACE ANTIGENS produced by these patients. Hepatitis D can occur either concomitantly with (coinfection) or subsequent to (superinfection) hepatitis B infection. Similar to hepatitis B, it is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 1.97 | 1 | 0 |
Aphakia Absence of crystalline lens totally or partially from field of vision, from any cause except after cataract extraction. Aphakia is mainly congenital or as result of LENS DISLOCATION AND SUBLUXATION. | 0 | 1.96 | 1 | 0 |
Hypothermia, Accidental [description not available] | 0 | 1.94 | 1 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 1.94 | 1 | 0 |
Behavior Disorders [description not available] | 0 | 1.94 | 1 | 0 |
Mental Disorders Psychiatric illness or diseases manifested by breakdowns in the adaptational process expressed primarily as abnormalities of thought, feeling, and behavior producing either distress or impairment of function. | 0 | 1.94 | 1 | 0 |
Brain Vascular Disorders [description not available] | 0 | 1.94 | 1 | 0 |
Amyotrophic Neuralgia [description not available] | 0 | 1.94 | 1 | 0 |
Cerebrovascular Disorders A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others. | 0 | 1.94 | 1 | 0 |
Brachial Plexus Neuritis A syndrome associated with inflammation of the BRACHIAL PLEXUS. Clinical features include severe pain in the shoulder region which may be accompanied by MUSCLE WEAKNESS and loss of sensation in the upper extremity. This condition may be associated with VIRUS DISEASES; IMMUNIZATION; SURGERY; heroin use (see HEROIN DEPENDENCE); and other conditions. The term brachial neuralgia generally refers to pain associated with brachial plexus injury. (From Adams et al., Principles of Neurology, 6th ed, pp1355-6) | 0 | 1.94 | 1 | 0 |
Marasmus [description not available] | 0 | 1.94 | 1 | 0 |
Protein-Energy Malnutrition The lack of sufficient energy or protein to meet the body's metabolic demands, as a result of either an inadequate dietary intake of protein, intake of poor quality dietary protein, increased demands due to disease, or increased nutrient losses. | 0 | 1.94 | 1 | 0 |
Acne Rosacea [description not available] | 0 | 1.94 | 1 | 0 |
Rosacea A cutaneous disorder primarily of convexities of the central part of the FACE, such as FOREHEAD; CHEEK; NOSE; and CHIN. It is characterized by FLUSHING; ERYTHEMA; EDEMA; RHINOPHYMA; papules; and ocular symptoms. It may occur at any age but typically after age 30. There are various subtypes of rosacea: erythematotelangiectatic, papulopustular, phymatous, and ocular (National Rosacea Society's Expert Committee on the Classification and Staging of Rosacea, J Am Acad Dermatol 2002; 46:584-7). | 0 | 1.94 | 1 | 0 |
Lipid Metabolism, Inborn Error [description not available] | 0 | 2.35 | 2 | 0 |
Focal Neurologic Deficits [description not available] | 0 | 1.94 | 1 | 0 |
Gargoylism, Hunter Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Mucopolysaccharidosis II Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15. | 0 | 1.94 | 1 | 0 |
Osseous Paget's Disease [description not available] | 0 | 1.94 | 1 | 0 |
Brittle Bone Disease [description not available] | 0 | 2.35 | 2 | 0 |
Cleidocranial Digital Dysostosis [description not available] | 0 | 1.94 | 1 | 0 |
Osteitis Deformans A disease marked by repeated episodes of increased bone resorption followed by excessive attempts at repair, resulting in weakened, deformed bones of increased mass. The resultant architecture of the bone assumes a mosaic pattern in which the fibers take on a haphazard pattern instead of the normal parallel symmetry. | 0 | 1.94 | 1 | 0 |
Osteogenesis Imperfecta COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I. | 0 | 2.35 | 2 | 0 |
Dermatitis, Occupational A recurrent contact dermatitis caused by substances found in the work place. | 0 | 1.94 | 1 | 0 |
Measles, German [description not available] | 0 | 1.94 | 1 | 0 |
Birth Injuries Mechanical or anoxic trauma incurred by the infant during labor or delivery. | 0 | 1.94 | 1 | 0 |
Congenital Syphilis [description not available] | 0 | 1.94 | 1 | 0 |
Syphilis, Congenital Syphilis acquired in utero and manifested by any of several characteristic tooth (Hutchinson's teeth) or bone malformations and by active mucocutaneous syphilis at birth or shortly thereafter. Ocular and neurologic changes may also occur. | 0 | 1.94 | 1 | 0 |
Femur Neck Fractures [description not available] | 0 | 1.94 | 1 | 0 |
Femoral Neck Fractures Fractures of the short, constricted portion of the thigh bone between the femur head and the trochanters. It excludes intertrochanteric fractures which are HIP FRACTURES. | 0 | 1.94 | 1 | 0 |
Kerion Celsi An inflammatory manifestation of tinea capitis with a pronounced swelling that develops into suppurative central and indurated peripheral area called kerion. | 0 | 1.94 | 1 | 0 |
Tinea Capitis Ringworm of the scalp and associated hair mainly caused by species of MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON, which may occasionally involve the eyebrows and eyelashes. | 0 | 1.94 | 1 | 0 |
Eye Manifestations Ocular disorders attendant upon non-ocular disease or injury. | 0 | 1.95 | 1 | 0 |
Calciphylaxes [description not available] | 0 | 1.94 | 1 | 0 |
Rachitis [description not available] | 0 | 3.26 | 2 | 0 |
Carbohydrate Metabolism, Inborn Error [description not available] | 0 | 2.64 | 3 | 0 |
Skin Manifestations Dermatologic disorders attendant upon non-dermatologic disease or injury. | 0 | 1.94 | 1 | 0 |
Addison's Disease [description not available] | 0 | 2.86 | 1 | 0 |
Addison Disease An adrenal disease characterized by the progressive destruction of the ADRENAL CORTEX, resulting in insufficient production of ALDOSTERONE and HYDROCORTISONE. Clinical symptoms include ANOREXIA; NAUSEA; WEIGHT LOSS; MUSCLE WEAKNESS; and HYPERPIGMENTATION of the SKIN due to increase in circulating levels of ACTH precursor hormone which stimulates MELANOCYTES. | 0 | 2.86 | 1 | 0 |
Impetigo Contagiosa [description not available] | 0 | 1.95 | 1 | 0 |
Impetigo A common superficial bacterial infection caused by STAPHYLOCOCCUS AUREUS or group A beta-hemolytic streptococci. Characteristics include pustular lesions that rupture and discharge a thin, amber-colored fluid that dries and forms a crust. This condition is commonly located on the face, especially about the mouth and nose. | 0 | 1.95 | 1 | 0 |
Tooth Resorption Resorption of calcified dental tissue, involving demineralization due to reversal of the cation exchange and lacunar resorption by osteoclasts. There are two types: external (as a result of tooth pathology) and internal (apparently initiated by a peculiar inflammatory hyperplasia of the pulp). (From Jablonski, Dictionary of Dentistry, 1992, p676) | 0 | 1.95 | 1 | 0 |
Arachnoid Membrane Inflammation [description not available] | 0 | 1.95 | 1 | 0 |
Avulsed Tooth [description not available] | 0 | 1.94 | 1 | 0 |
Albers-Schoenberg Disease [description not available] | 0 | 1.94 | 1 | 0 |
Osteopetrosis Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY). | 0 | 1.94 | 1 | 0 |
Acute Rheumatic Fever [description not available] | 0 | 1.95 | 1 | 0 |
Esophageal Stricture [description not available] | 0 | 1.95 | 1 | 0 |
Deficiency, Vitamin B [description not available] | 0 | 1.95 | 1 | 0 |
Diaphragmatic Hernia [description not available] | 0 | 1.95 | 1 | 0 |
Esophageal Stenosis A stricture of the ESOPHAGUS. Most are acquired but can be congenital. | 0 | 1.95 | 1 | 0 |
Vitamin B Deficiency A condition due to deficiency in any member of the VITAMIN B COMPLEX. These B vitamins are water-soluble and must be obtained from the diet because they are easily lost in the urine. Unlike the lipid-soluble vitamins, they cannot be stored in the body fat. | 0 | 1.95 | 1 | 0 |
Anemia, Macrocytic Anemia characterized by larger than normal erythrocytes, increased mean corpuscular volume (MCV) and increased mean corpuscular hemoglobin (MCH). | 0 | 1.94 | 1 | 0 |
Infections, Trichomonas [description not available] | 0 | 2.86 | 1 | 0 |
Trichomonas Infections Infections in birds and mammals produced by various species of Trichomonas. | 0 | 2.86 | 1 | 0 |
Myelopathy [description not available] | 0 | 1.94 | 1 | 0 |
Spinal Cord Diseases Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord. | 0 | 1.94 | 1 | 0 |
Tuberculosis, Renal Infection of the KIDNEY with species of MYCOBACTERIUM. | 0 | 1.94 | 1 | 0 |
Oral Manifestations Disorders of the mouth attendant upon non-oral disease or injury. | 0 | 2.85 | 1 | 0 |
Kwashiorkor A syndrome produced by severe protein deficiency, characterized by retarded growth, changes in skin and hair pigment, edema, and pathologic changes in the liver, including fatty infiltration, necrosis, and fibrosis. The word is a local name in Gold Coast, Africa, meaning displaced child. Although first reported from Africa, kwashiorkor is now known throughout the world, but mainly in the tropics and subtropics. It is considered to be related to marasmus. (From Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Pellagra A disease due to deficiency of NIACIN, a B-complex vitamin, or its precursor TRYPTOPHAN. It is characterized by scaly DERMATITIS which is often associated with DIARRHEA and DEMENTIA (the three D's). | 0 | 2.35 | 2 | 0 |
Allergy, Drug [description not available] | 0 | 1.94 | 1 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 1.94 | 1 | 0 |
Hyperthyroid [description not available] | 0 | 1.94 | 1 | 0 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 1.94 | 1 | 0 |
Deficiency, Folic Acid [description not available] | 0 | 1.94 | 1 | 0 |
Folic Acid Deficiency A nutritional condition produced by a deficiency of FOLIC ACID in the diet. Many plant and animal tissues contain folic acid, abundant in green leafy vegetables, yeast, liver, and mushrooms but destroyed by long-term cooking. Alcohol interferes with its intermediate metabolism and absorption. Folic acid deficiency may develop in long-term anticonvulsant therapy or with use of oral contraceptives. This deficiency causes anemia, macrocytic anemia, and megaloblastic anemia. It is indistinguishable from vitamin B 12 deficiency in peripheral blood and bone marrow findings, but the neurologic lesions seen in B 12 deficiency do not occur. (Merck Manual, 16th ed) | 0 | 1.94 | 1 | 0 |
Nutritional Disorders [description not available] | 0 | 1.94 | 1 | 0 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 1.94 | 1 | 0 |
Ectropion The turning outward (eversion) of the edge of the eyelid, resulting in the exposure of the palpebral conjunctiva. (Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Lathyrism A paralytic condition of the legs caused by ingestion of lathyrogens, especially BETA-AMINOPROPIONITRILE or beta-N-oxalyl amino-L-alanine, which are found in the seeds of plants of the genus LATHYRUS. | 0 | 1.94 | 1 | 0 |
Abnormalities, Drug-Induced Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment. | 0 | 2.94 | 4 | 0 |