Orphanet Database · Orphadata CC-BY-4.0
Rare (orphan) diseases
The full catalogue of 7,547 diseases with genetics, phenotypes, epidemiology, orphan drugs, and clinical trials.
7,547
Diseases
4 552
Genes
8 700
Phenotypes
140
Regions
All (7,547)Bio anomalyCategoryClinical groupClinical subtypeClinical syndromeDiseaseEtiological subtypeHistopathological subtypeMalformationMorphological anomalyClinical situation
ALK-negative anaplastic large cell lymphoma
Not applicable
Adult
ALK-positive anaplastic large cell lymphoma
Not applicable
Adolescent, Adult, Childhood
Anaplastic/large cell medulloblastoma
Infancy, Neonatal
C3 glomerulonephritis
Autosomal dominant
Classic Hodgkin lymphoma, lymphocyte-depleted type
Adult
Classic Hodgkin lymphoma, lymphocyte-rich type
Adult
Classic Hodgkin lymphoma, mixed cellularity type
Adult
Classic Hodgkin lymphoma, nodular sclerosis type
Adult
Classic medulloblastoma
Childhood
Clear cell papillary renal cell carcinoma
Dedifferentiated liposarcoma
Not applicable
Adult
Dense deposit disease
Autosomal recessive
Childhood
Desmoplastic/nodular medulloblastoma
Not applicable
Adult
Fibrillary astrocytoma
Gemistocytic astrocytoma
Giant cell glioblastoma
Not applicable
Adult
Gliosarcoma
Not applicable
Adult
Hepatoportal sclerosis
All ages
Isolated focal cortical dysplasia type IIa
Not applicable
Isolated focal cortical dysplasia type IIb
Not applicable
Isolated focal cortical dysplasia type Ia
Not applicable