| Condition | Indicated | Relationship Strength | Studies | Trials |
|---|
Acute Myelogenous Leukemia
[description not available] | 0 | 9.89 | 51 | 6 |
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 | 9.89 | 51 | 6 |
Graft-Versus-Host Disease
[description not available] | 0 | 2.08 | 1 | 0 |
Local Neoplasm Recurrence
[description not available] | 0 | 2.69 | 3 | 0 |
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 | 2.08 | 1 | 0 |
Benign Neoplasms
[description not available] | 0 | 4.46 | 5 | 1 |
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 | 4.46 | 5 | 1 |
Aspergillus Infection
[description not available] | 0 | 2.07 | 1 | 0 |
Nasal Catarrh
[description not available] | 0 | 2.07 | 1 | 0 |
Sinus Infections
[description not available] | 0 | 2.07 | 1 | 0 |
Aspergillosis
Infections with fungi of the genus ASPERGILLUS. | 0 | 2.07 | 1 | 0 |
Rhinitis
Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 2.07 | 1 | 0 |
Sinusitis
Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 2.07 | 1 | 0 |
Chloroma
[description not available] | 0 | 2.72 | 3 | 0 |
Cancer of Skin
[description not available] | 0 | 2.07 | 1 | 0 |
Chromosomal Translocation
[description not available] | 0 | 2.77 | 3 | 0 |
Skin Neoplasms
Tumors or cancer of the SKIN. | 0 | 2.07 | 1 | 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 | 2.72 | 3 | 0 |
Recrudescence
[description not available] | 0 | 7.18 | 10 | 4 |
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 | 2.48 | 2 | 0 |
Granulocytic Leukemia
[description not available] | 0 | 7.51 | 19 | 8 |
Acute Disease
Disease having a short and relatively severe course. | 0 | 9.95 | 33 | 10 |
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 | 7.51 | 19 | 8 |
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 | 2.42 | 2 | 0 |
Acute Lymphoid Leukemia
[description not available] | 0 | 5.67 | 7 | 1 |
Diffuse Mixed Small and Large Cell Lymphoma
[description not available] | 0 | 5.42 | 8 | 2 |
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 | 5.42 | 8 | 2 |
Precursor Cell Lymphoblastic Leukemia-Lymphoma
A neoplasm characterized by abnormalities of the lymphoid cell precursors leading to excessive lymphoblasts in the marrow and other organs. It is the most common cancer in children and accounts for the vast majority of all childhood leukemias. | 0 | 5.67 | 7 | 1 |
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 | 2.01 | 1 | 0 |
Disease Exacerbation
[description not available] | 0 | 2.69 | 3 | 0 |
Perforated Appendicitis
[description not available] | 0 | 2.01 | 1 | 0 |
Appendicitis
Acute inflammation of the APPENDIX. Acute appendicitis is classified as simple, gangrenous, or perforated. | 0 | 2.01 | 1 | 0 |
Allergy, Drug
[description not available] | 0 | 2.39 | 2 | 0 |
Leucocythaemia
[description not available] | 0 | 9.11 | 28 | 5 |
Hives
[description not available] | 0 | 2.01 | 1 | 0 |
Drug Hypersensitivity
Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 2.39 | 2 | 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 | 9.11 | 28 | 5 |
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 | 2.01 | 1 | 0 |
Leukocytosis
A transient increase in the number of leukocytes in a body fluid. | 0 | 5.76 | 4 | 2 |
Embolism, Pulmonary
[description not available] | 0 | 2.01 | 1 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura
[description not available] | 0 | 2.01 | 1 | 0 |
Acute Promyelocytic Leukemia
[description not available] | 0 | 7.34 | 12 | 4 |
Pulmonary Embolism
Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 2.01 | 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 | 2.01 | 1 | 0 |
Leukemia, Promyelocytic, Acute
An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 7.34 | 12 | 4 |
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 | 2.94 | 1 | 0 |
Dysmyelopoietic Syndromes
[description not available] | 0 | 4.15 | 6 | 0 |
Myelodysplastic Syndromes
Clonal hematopoietic stem cell disorders characterized by dysplasia in one or more hematopoietic cell lineages. They predominantly affect patients over 60, are considered preleukemic conditions, and have high probability of transformation into ACUTE MYELOID LEUKEMIA. | 0 | 4.15 | 6 | 0 |
A-V Dissociation
[description not available] | 0 | 2.02 | 1 | 0 |
Germinoblastoma
[description not available] | 0 | 5.01 | 5 | 2 |
Lymphoma
A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 5.01 | 5 | 2 |
Leukemia, Acute Monocytic
[description not available] | 0 | 2.88 | 4 | 0 |
Leukemia, Monocytic, Acute
An acute myeloid leukemia in which 80% or more of the leukemic cells are of monocytic lineage including monoblasts, promonocytes, and MONOCYTES. | 0 | 2.88 | 4 | 0 |
Leukemia, Lymphocytic
[description not available] | 0 | 4.27 | 4 | 1 |
Leukemia, Lymphoid
Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 4.27 | 4 | 1 |
Granuloma, Hodgkin
[description not available] | 0 | 3.76 | 2 | 1 |
Angioimmunoblastic Lymphadenopathy
[description not available] | 0 | 3.76 | 2 | 1 |
Diffuse Large B-Cell Lymphoma
[description not available] | 0 | 2.38 | 2 | 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 | 3.76 | 2 | 1 |
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 | 3.76 | 2 | 1 |
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 | 2.38 | 2 | 0 |
Remission, Spontaneous
A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 1.95 | 1 | 0 |
Leukemia L 1210
[description not available] | 0 | 4.13 | 6 | 0 |
Pregnancy
The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 2.37 | 2 | 0 |
Palsy
[description not available] | 0 | 1.98 | 1 | 0 |
Symptom Cluster
[description not available] | 0 | 3.78 | 2 | 1 |
Benign Cranial Nerve Neoplasms
[description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Syndrome
A characteristic symptom complex. | 0 | 3.78 | 2 | 1 |
Infectious Diseases
[description not available] | 0 | 3.37 | 1 | 1 |
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 | 3.37 | 1 | 1 |
Leukemia P388
An experimental lymphocytic leukemia originally induced in DBA/2 mice by painting with methylcholanthrene. | 0 | 2.67 | 3 | 0 |
Complications, Neoplastic Pregnancy
[description not available] | 0 | 1.98 | 1 | 0 |
Fetal Growth Restriction
[description not available] | 0 | 1.98 | 1 | 0 |
Fetal Growth Retardation
Failure of a FETUS to attain expected GROWTH. | 0 | 1.98 | 1 | 0 |
Anterior Choroidal Artery Infarction
[description not available] | 0 | 1.98 | 1 | 0 |
Cerebral Infarction
The formation of an area of NECROSIS in the CEREBRUM caused by an insufficiency of arterial or venous blood flow. Infarcts of the cerebrum are generally classified by hemisphere (i.e., left vs. right), lobe (e.g., frontal lobe infarction), arterial distribution (e.g., INFARCTION, ANTERIOR CEREBRAL ARTERY), and etiology (e.g., embolic infarction). | 0 | 1.98 | 1 | 0 |
Cancer of Mediastinum
[description not available] | 0 | 2.9 | 1 | 0 |
Mediastinal Neoplasms
Tumors or cancer of the MEDIASTINUM. | 0 | 2.9 | 1 | 0 |
Gasser Syndrome
[description not available] | 0 | 1.98 | 1 | 0 |
Leukemia, Myeloid, Acute, M4
[description not available] | 0 | 2.67 | 3 | 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 | 1.98 | 1 | 0 |
Leukemia, Myelomonocytic, Acute
A pediatric acute myeloid leukemia involving both myeloid and monocytoid precursors. At least 20% of non-erythroid cells are of monocytic origin. | 0 | 2.67 | 3 | 0 |
Chromosome Deletion
Actual loss of portion of a chromosome. | 0 | 1.98 | 1 | 0 |
B-Cell Lymphoma
[description not available] | 0 | 1.99 | 1 | 0 |
T-Cell Lymphoma
[description not available] | 0 | 1.99 | 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 | 1.99 | 1 | 0 |
Lymphoma, T-Cell
A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 1.99 | 1 | 0 |
Agranulocytosis
A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS). | 0 | 1.99 | 1 | 0 |
Coagulation, Disseminated Intravascular
[description not available] | 0 | 1.99 | 1 | 0 |
Hematoma, Subdural
Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 1.99 | 1 | 0 |
Disseminated Intravascular Coagulation
A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clotting mechanism may arise from any of a number of disorders. A majority of the patients manifest skin lesions, sometimes leading to PURPURA FULMINANS. | 0 | 1.99 | 1 | 0 |
African Lymphoma
[description not available] | 0 | 2.91 | 1 | 0 |
Mandibular Neoplasms
Tumors or cancer of the MANDIBLE. | 0 | 2.91 | 1 | 0 |
Burkitt Lymphoma
A form of undifferentiated malignant LYMPHOMA usually found in central Africa, but also reported in other parts of the world. It is commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass. B-cell antigens are expressed on the immature cells that make up the tumor in virtually all cases of Burkitt lymphoma. The Epstein-Barr virus (HERPESVIRUS 4, HUMAN) has been isolated from Burkitt lymphoma cases in Africa and it is implicated as the causative agent in these cases; however, most non-African cases are EBV-negative. | 0 | 2.91 | 1 | 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 | 2.91 | 1 | 0 |
Elevated Cholesterol
[description not available] | 0 | 4.3 | 1 | 1 |
Cheilitis
Inflammation of the lips. It is of various etiologies and degrees of pathology. | 0 | 4.3 | 1 | 1 |
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 | 4.3 | 1 | 1 |
Hypertriglyceridemia
A condition of elevated levels of TRIGLYCERIDES in the blood. | 0 | 4.3 | 1 | 1 |
Absence Seizure
[description not available] | 0 | 2 | 1 | 0 |
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 | 1 | 0 |
Blast Phase
[description not available] | 0 | 3.3 | 2 | 0 |
Granulocytic Leukemia, Chronic
[description not available] | 0 | 3.79 | 2 | 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 | 3.3 | 2 | 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 | 3.79 | 2 | 0 |
Benign Neoplasms, Brain
[description not available] | 0 | 2.38 | 2 | 0 |
Central Nervous System Neoplasm
[description not available] | 0 | 2 | 1 | 0 |
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 | 2.38 | 2 | 0 |
Central Nervous System Neoplasms
Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 2 | 1 | 0 |
Di Guglielmo Disease
[description not available] | 0 | 2 | 1 | 0 |
Infection
[description not available] | 0 | 2 | 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 | 2 | 1 | 0 |
Infections
Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 2 | 1 | 0 |
Neutropenia
A decrease in the number of NEUTROPHILS found in the blood. | 0 | 2 | 1 | 0 |
Tachycardia, Supraventricular
A generic expression for any tachycardia that originates above the BUNDLE OF HIS. | 0 | 2 | 1 | 0 |
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 | 2 | 1 | 0 |
Chromosomal Triplication
[description not available] | 0 | 2 | 1 | 0 |
Cancer, Second Primary
[description not available] | 0 | 2 | 1 | 0 |
Polyploid
[description not available] | 0 | 2.92 | 1 | 0 |
Refractory Anemia
[description not available] | 0 | 1.98 | 1 | 0 |
Hemorrhagic Thrombocythemia
[description not available] | 0 | 1.98 | 1 | 0 |
Anemia, Refractory
A severe sometimes chronic anemia, usually macrocytic in type, that does not respond to ordinary antianemic therapy. | 0 | 1.98 | 1 | 0 |
Thrombocythemia, Essential
A clinical syndrome characterized by repeated spontaneous hemorrhages and a remarkable increase in the number of circulating platelets. | 0 | 1.98 | 1 | 0 |
Leukocytopenia
[description not available] | 0 | 2.66 | 3 | 0 |
Leukopenia
A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 2.66 | 3 | 0 |
EHS Tumor
[description not available] | 0 | 1.98 | 1 | 0 |
ATLL
[description not available] | 0 | 3.36 | 1 | 1 |
Leukemia-Lymphoma, Adult T-Cell
Aggressive T-Cell malignancy with adult onset, caused by HUMAN T-LYMPHOTROPIC VIRUS 1. It is endemic in Japan, the Caribbean basin, Southeastern United States, Hawaii, and parts of Central and South America and sub-Saharan Africa. | 0 | 3.36 | 1 | 1 |
Arrhythmia
[description not available] | 0 | 1.98 | 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 | 1.98 | 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 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
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 | 1.97 | 1 | 0 |
Carcinoma, Epidermoid
[description not available] | 0 | 1.97 | 1 | 0 |
Cancer of Ovary
[description not available] | 0 | 2.38 | 2 | 0 |
Dysembryoma
[description not available] | 0 | 1.97 | 1 | 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 | 2.38 | 2 | 0 |
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 | 1.97 | 1 | 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 | 2.38 | 2 | 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 | 1.97 | 1 | 0 |
Experimental Leukemia
[description not available] | 0 | 1.97 | 1 | 0 |
Afibrinogenemia, Congenital
[description not available] | 0 | 2.89 | 1 | 0 |
Afibrinogenemia
A deficiency or absence of FIBRINOGEN in the blood. | 0 | 2.89 | 1 | 0 |
Myelomonocytic Leukemia, Chronic
[description not available] | 0 | 2.37 | 2 | 0 |
Leukemia, Myelomonocytic, Chronic
A myelodysplastic-myeloproliferative disease characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood. | 0 | 2.37 | 2 | 0 |
Abnormalities, Autosome
[description not available] | 0 | 1.97 | 1 | 0 |
Preleukemia
Conditions in which the abnormalities in the peripheral blood or bone marrow represent the early manifestations of acute leukemia, but in which the changes are not of sufficient magnitude or specificity to permit a diagnosis of acute leukemia by the usual clinical criteria. | 0 | 2.37 | 2 | 0 |
Thrombopenia
[description not available] | 0 | 2.37 | 2 | 0 |
Thrombocytopenia
A subnormal level of BLOOD PLATELETS. | 0 | 2.37 | 2 | 0 |
Hematuria
Presence of blood in the urine. | 0 | 3.35 | 1 | 1 |
Cancer of Colon
[description not available] | 0 | 4.32 | 2 | 2 |
Cancer of Liver
[description not available] | 0 | 3.35 | 1 | 1 |
Cancer of Spleen
[description not available] | 0 | 3.35 | 1 | 1 |
Cancer of Stomach
[description not available] | 0 | 4.32 | 2 | 2 |
Colonic Neoplasms
Tumors or cancer of the COLON. | 0 | 4.32 | 2 | 2 |
Liver Neoplasms
Tumors or cancer of the LIVER. | 0 | 3.35 | 1 | 1 |
Stomach Neoplasms
Tumors or cancer of the STOMACH. | 0 | 4.32 | 2 | 2 |
Aplasia Pure Red Cell
[description not available] | 0 | 1.97 | 1 | 0 |
Red-Cell Aplasia, Pure
Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. | 0 | 1.97 | 1 | 0 |
Benign Meningeal Neoplasms
[description not available] | 0 | 1.97 | 1 | 0 |
Cancer of Testis
[description not available] | 0 | 1.97 | 1 | 0 |
Meningeal Neoplasms
Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 1.97 | 1 | 0 |
Testicular Neoplasms
Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 1.97 | 1 | 0 |
Acute Edematous Pancreatitis
[description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Primary Peritonitis
[description not available] | 0 | 1.97 | 1 | 0 |
Cancer of the Uterus
[description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Uterine Neoplasms
Tumors or cancer of the UTERUS. | 0 | 1.97 | 1 | 0 |
Leukemia, Smoldering
[description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Acute Liver Injury, Drug-Induced
[description not available] | 0 | 1.96 | 1 | 0 |
Liver Dysfunction
[description not available] | 0 | 1.96 | 1 | 0 |
Liver Diseases
Pathological processes of the LIVER. | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Aging
The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 1.97 | 1 | 0 |
Cancer of Lung
[description not available] | 0 | 3.35 | 1 | 1 |
Lung Neoplasms
Tumors or cancer of the LUNG. | 0 | 3.35 | 1 | 1 |
Dermatoses
[description not available] | 0 | 1.96 | 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 | 2.37 | 2 | 0 |
Diarrhea
An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 1.96 | 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 | 1.96 | 1 | 0 |
Skin Diseases
Diseases involving the DERMIS or EPIDERMIS. | 0 | 1.96 | 1 | 0 |
Alopecia Cicatrisata
[description not available] | 0 | 1.96 | 1 | 0 |
Alopecia
Absence of hair from areas where it is normally present. | 0 | 1.96 | 1 | 0 |