Disease Index
9,486 diseasesintractable diarrhea-choanal atresia-eye anomalies syndrome
intrahepatic cholestasis
medical condition
MeSH: D002780
intrahepatic cholestasis of pregnancy
intrahepatic cholestasis characterized by reversible cholestasis typically occurring in the second or third trimester of pregnancy, elevated serum aminotransferases and bile acid level and resolution of symptoms by 2 to 3 weeks after delivery
MeSH: C535932
intralobar congenital pulmonary sequestration
human disease
Intramural coronary arterial course
human disease
intraneural perineurioma
Human disease
intraocular medulloepithelioma
Intraretinal microvascular abnormalities
medical condition
intrauterine growth restriction-short stature-early adult-onset diabetes syndrome
human disease
Intravascular large B-cell lymphoma
medical condition
Invasive hydatidiform mole
complete hydatidiform mole or very rarely a partial mole that invades the myometrium
MeSH: D002820
invasive non-typhoidal salmonellosis
Inverse Klippel-Trenaunay syndrome
human disease
Inverse Marcus-Gunn phenomenon
IRIDA syndrome
Iron-refractory iron deficiency anemia
iridocorneal endothelial syndrome
medical condition
MeSH: D057129
iridogoniodysgenesis syndrome
Human disease
iron metabolism disease
Human disease
MeSH: D019189
IRVAN syndrome
human disease
ischio-vertebral syndrome
Ischio-vertebral syndrome is a very rare, poorly-defined bone disease characterized by ischial aplasia or hypoplasia, vertebral anomalies (vertebral malsegmentation, kyphoscoliosis), and in some patients, non-distinctive facial dysmorphism
ischiopatellar dysplasia
Small patella syndrome (SPS) is a very rare benign bone dysplasia affecting skeletal structures of the lower limb and the pelvis
MeSH: C535540
islet cell carcinoma
islet cell tumor that has material basis in epithelial cells
MeSH: D018273
Isobutyryl-coenzyme A dehydrogenase deficiency
gene (11q25)
MeSH: C535541
isochromosome Y
human disease
isochromosomy Yp
human disease
isochromosomy Yq
human disease
Isodicentric 15
medical condition
MeSH: C580205
isolated agammaglobulinemia
Isolated agammaglobulinemia (IA) is the non-syndromic form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy
isolated agenesis of gallbladder
human disease
MeSH: C562564
isolated anhidrosis with normal sweat glands
anhidrosis that has material basis in homozygous mutation in the ITPR2 gene on chromosome 12p11