Disease Index

9,486 diseases
acute myeloid leukemia with t(9;11)(p22;q23)
human disease
acute myelomonocytic leukemia
acute leukemia characterized by the proliferation of both neutrophil and monocyte precursors
MeSH: D015479
acute necrotizing encephalopathy of childhood
acute neonatal citrullinemia type 1
acute pandysautonomia
human disease
Acute panmyelosis with myelofibrosis
acute myeloid leukemia characterized by bone marrow fibrosis without preexisting primary myelofibrosis
ICD: C94.4
acute poisoning by drugs with membrane-stabilizing effect
Acute poisoning with a membrane-stabilizing effect is potentially life-threatening. The principle drugs involved are tricyclic antidepressants, chloroquine, some types of beta blockers, class IA antiarrhythmics, carbamazepin and cocaine.
acute promyelocytic leukemia
acute myeloid leukemia characterized by accumulation of promyelocytes in the bone marrow and by a translocation between chromosomes 15 and 17
MeSH: D015473
acute pure sensory neuropathy
human disease
acute sensory ataxic neuropathy
human disease
acute undifferentiated leukemia
rare acute leukemia of ambiguous lineage in which the blasts do not express markers specific to myeloid or lymphoid lineage
acyl-CoA dehydrogenase 9 deficiency
Acyl-CoA dehydrogenase 9 (ACAD9) deficiency is a rare disorder leading to a deficiency of complex I of the respiratory chain and is characterized by neurological dysfunction, hepatic failure and cardiomyopathy
MeSH: C567006
acyl-CoA dehydrogenase deficiency
human disease
adactyly of foot
human disease
adactyly of foot, bilateral
human disease
adactyly of foot, unilateral
human disease
adactyly of hand
human disease
adamantinoma
bone cancer that is located in almost exclusively in the long bones
MeSH: D050398
Adams-Oliver syndrome
syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs
MeSH: C538225
ADan amyloidosis
cerebral amyloid angiopathy characterized by ataxia, intention tremor, psychosis and dementia that has material basis in an autosomal dominant mutation of ITM2B on chromosome 13q14.2
MeSH: C538209
Addison's disease
adrenal cortical hypofunction that is characterized by insufficient steroid hormone production by the adrenal glands
MeSH: D000224
Adducted thumb syndrome
rare genetic disease affecting palate, thumbs, and upper limbs
adenine phosphoribosyltransferase deficiency
amino acid metabolic disorder characterized by the formation 2,8-dihydroxyadenine stones and renal failure secondary to intratubular crystalline precipitation. It has an autosomal recessive inheritance pattern
ICD: E79MeSH: C538228
adenocarcinoma of gallbladder and extrahepatic biliary tract
human disease
adenocarcinoma of liver and intrahepatic biliary tract
human disease
adenocarcinoma of penis
adenocarcinoma that involves the penis
adenohypophysitis
autoimmune disease of the pituitary gland which can present with varying degrees of pituitary hormonal impairment and/or with symptoms related to pituitary enlargement. It predominantly affects young women in pregnancy or the peripartum period
adenoid basal carcinoma of the cervix uteri
skin adenoid basal cell carcinoma that involves the uterine cervix
adenoid cystic carcinoma of the cervix uteri
adenoid cystic carcinoma that involves the uterine cervix
adenoid cystic carcinoma of the corpus uteri
adenoid cystic carcinoma that involves the body of uterus
Page 12 of 317 (9,486 total)