Disease Index
9,486 diseasesaggressive primary cutaneous B-cell lymphoma
human disease
aggressive primary cutaneous T-cell lymphoma
human disease
aggressive systemic mastocytosis
Human disease
agnathia-otocephaly complex
Human disease
MeSH: C562503
AH amyloidosis
human disease
AICA-ribosiduria
MeSH: C563876
Aicardi syndrome
syndrome that is characterized by absence or underdeveloped tissue connecting the left and right halves of the brain, infantile spasms and chorioretinal lacunae, which are defects in the light-sensitive tissue at the back of the eye
MeSH: D058540
Aicardi-Goutieres syndrome
a rare genetic neurodevelopmental disorder
MeSH: C535607
AIS2
human disease
AIS3
human disease
AIS4
human disease
AKT2-related familial partial lipodystrophy
human disease
AL amyloidosis
medical condition
ICD: E85MeSH: D000075363
Al Gazali syndrome
MeSH: C536817
Alagille syndrome
congenital disorder of digestive system
MeSH: D016738
Alagille syndrome due to 20p12 microdeletion
human disease
alar cartilages hypoplasia-coloboma-telecanthus syndrome
MeSH: C535967
albinism–deafness syndrome
medical condition
albinism, oculocutaneous, 8
human disease
Albright's hereditary osteodystrophy
osteochondrodysplasia that has material basis in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face
ICD: E20.1
Aldolase A deficiency
medical condition
ICD: E74.1MeSH: C562718
aldosterone-producing adenoma with seizures and neurological abnormalities
human disease
aldosterone-producing adrenal cortex adenoma
adenoma of the adrenal cortex that produces aldosterone. It may be associated with Conn syndrome. Clinical presentation includes hypertension, hypokalemia, and muscle weakness
Aldred syndrome
medical condition
aleukemic mast cell leukemia
human disease
Alexander disease
congenital disorder of nervous system
ICD: E75.2MeSH: D038261
Alexander disease type I
Alexander disease type II
Alexander disease type II (AxD type II) is an astrogliopathy and a form of Alexander disease (AxD; see this term) characterized by ataxia, bulbar symptoms, spastic paraparesis, palatal myoclonus, and autonomic symptoms
ALG1-CDG
medical condition
ALK-negative anaplastic large cell lymphoma