MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Argyria

ORPHA:60014Disease
Not applicable

Aromatase deficiency

ORPHA:91Disease
Autosomal recessive

Aromatase excess syndrome

ORPHA:178345Disease
Autosomal dominant

Aromatic L-amino acid decarboxylase deficiency

ORPHA:35708Disease
Autosomal recessive

Arthrochalasia Ehlers-Danlos syndrome

ORPHA:1899Disease
Autosomal dominant

Asbestos intoxication

ORPHA:2302Disease

Aseptic abscess syndrome

ORPHA:54251Disease
Not applicable

Asherman syndrome

ORPHA:137686Disease
Not applicable

Aspartylglucosaminuria

ORPHA:93Disease
Autosomal recessive

Aspergillosis

ORPHA:1163Disease
Not applicable

Astroblastoma

ORPHA:251679Disease
Not applicable

Asymptomatic hyperCKemia-myalgia-rhabdomyolysis syndrome

ORPHA:689021Disease
Autosomal recessive

Ataxia with vitamin E deficiency

ORPHA:96Disease
Autosomal recessive

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-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

Athabaskan brainstem dysgenesis syndrome

ORPHA:69739Disease
Autosomal recessive

Atopic keratoconjunctivitis

ORPHA:163934Disease
Not applicable

Atrichia with papular lesions

ORPHA:86819Disease
Autosomal recessive