| Condition | Indicated | Relationship Strength | Studies | Trials |
|---|
HIV Coinfection
[description not available] | 0 | 2.25 | 1 | 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 | 2.25 | 1 | 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 | 2.25 | 1 | 0 |
Autoimmune Chronic Hepatitis
[description not available] | 0 | 2.21 | 1 | 0 |
Hepatitis, Autoimmune
A chronic self-perpetuating hepatocellular INFLAMMATION of unknown cause, usually with HYPERGAMMAGLOBULINEMIA and serum AUTOANTIBODIES. | 0 | 2.21 | 1 | 0 |
Becker Muscular Dystrophy
[description not available] | 0 | 2.1 | 1 | 0 |
Agitation, Psychomotor
[description not available] | 0 | 2.1 | 1 | 0 |
Developmental Psychomotor Disorders
[description not available] | 0 | 2.1 | 1 | 0 |
Psychomotor Agitation
A feeling of restlessness associated with increased motor activity. This may occur as a manifestation of nervous system drug toxicity or other conditions. | 0 | 2.1 | 1 | 0 |
Muscular Dystrophy, Duchenne
An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) | 0 | 2.1 | 1 | 0 |
Recrudescence
[description not available] | 0 | 2.11 | 1 | 0 |
Adenoma, alpha-Cell
[description not available] | 0 | 2.11 | 1 | 0 |
Cancer of Pancreas
[description not available] | 0 | 2.11 | 1 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura
[description not available] | 0 | 2.11 | 1 | 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 | 2.11 | 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 | 2.11 | 1 | 0 |
Disease Exacerbation
[description not available] | 0 | 2.06 | 1 | 0 |
Berger Disease
[description not available] | 0 | 2.06 | 1 | 0 |
Alcoholic Cirrhosis
[description not available] | 0 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Liver Cirrhosis, Alcoholic
FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 2.06 | 1 | 0 |
Respiration Disorders
Diseases of the respiratory system in general or unspecified or for a specific respiratory disease not available. | 0 | 1.93 | 1 | 0 |
Asthma, Bronchial
[description not available] | 0 | 2.34 | 2 | 0 |
Centriacinar Emphysema
[description not available] | 0 | 1.93 | 1 | 0 |
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 | 2.34 | 2 | 0 |
Polyarthritis
[description not available] | 0 | 2.63 | 3 | 0 |
Rheumatoid Arthritis
[description not available] | 0 | 2.86 | 4 | 0 |
Arthritis
Acute or chronic inflammation of JOINTS. | 0 | 2.63 | 3 | 0 |
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 | 2.86 | 4 | 0 |
Pyrexia
[description not available] | 0 | 1.93 | 1 | 0 |
Innate Inflammatory Response
[description not available] | 0 | 1.93 | 1 | 0 |
Fever
An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 1.93 | 1 | 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 | 1.93 | 1 | 0 |
Leucocythaemia
[description not available] | 0 | 1.93 | 1 | 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 | 1.93 | 1 | 0 |
Nephrosis
Pathological processes of the KIDNEY without inflammatory or neoplastic components. Nephrosis may be a primary disorder or secondary complication of other diseases. It is characterized by the NEPHROTIC SYNDROME indicating the presence of PROTEINURIA and HYPOALBUMINEMIA with accompanying EDEMA. | 0 | 1.93 | 1 | 0 |
Acute Rheumatic Fever
[description not available] | 0 | 1.94 | 1 | 0 |
Rheumatism
[description not available] | 0 | 1.94 | 1 | 0 |
Rheumatic Diseases
Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 1.94 | 1 | 0 |
Community Acquired Infection
[description not available] | 0 | 2.03 | 1 | 0 |
Acute Respiratory Distress Syndrome
[description not available] | 0 | 2.03 | 1 | 0 |
Pneumonia, Pneumococcal
A febrile disease caused by STREPTOCOCCUS PNEUMONIAE. | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Amnionitis
[description not available] | 0 | 1.99 | 1 | 0 |
Labor, Premature
[description not available] | 0 | 1.99 | 1 | 0 |
Infantile Respiratory Distress Syndrome
[description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Respiratory Distress Syndrome, Newborn
A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause. | 0 | 1.99 | 1 | 0 |