MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Aseptic abscess syndrome

ORPHA:54251Disease
Not applicable

Asherman syndrome

ORPHA:137686Disease
Not applicable

Aspartylglucosaminuria

ORPHA:93Disease
Autosomal recessive

Aspergillosis

ORPHA:1163Disease
Not applicable

Astley-Kendall dysplasia

ORPHA:85175Malform.
Autosomal recessive

Astroblastoma

ORPHA:251679Disease
Not applicable

Astrocytoma

ORPHA:94Clin. grp.

Asymptomatic hyperCKemia-myalgia-rhabdomyolysis syndrome

ORPHA:689021Disease
Autosomal recessive

Ataxia with vitamin E deficiency

ORPHA:96Disease
Autosomal recessive

Ataxia-deafness-intellectual disability syndrome

ORPHA:1188Malform.
Unknown

Ataxia-hypogonadism-choroidal dystrophy syndrome

ORPHA:1180Disease
Autosomal recessive

Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome

ORPHA:370022Disease
Autosomal recessive

Ataxia-oculomotor apraxia type 1

ORPHA:1168Disease
Autosomal recessive

Ataxia-oculomotor apraxia type 4

ORPHA:459033Disease
Autosomal recessive

Ataxia-pancytopenia syndrome

ORPHA:2585Malform.
Autosomal dominant

Ataxia-photosensitivity-short stature syndrome

ORPHA:1184Malform.
Unknown

Ataxia-tapetoretinal degeneration syndrome

ORPHA:1178Disease
Unknown

Ataxia-telangiectasia

ORPHA:100Disease
Autosomal recessive

Ataxia-telangiectasia variant

ORPHA:370109Disease
Autosomal recessive

Ataxia-telangiectasia-like disorder

ORPHA:251347Disease
Autosomal recessive

Atelosteogenesis type I

ORPHA:1190Malform.
Autosomal dominant

Atelosteogenesis type II

ORPHA:56304Malform.
Autosomal recessive

Atelosteogenesis type III

ORPHA:56305Malform.
Autosomal dominant, Not applicable

Athabaskan brainstem dysgenesis syndrome

ORPHA:69739Disease
Autosomal recessive