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
Functioning neuroendocrine tumor of pancreas
Adult, Elderly
Galactosemia
Autosomal recessive
Childhood, Infancy, Neonatal
Genetic congenital malformation of the eye with glaucoma as a major feature
Neonatal
Genetic peripheral neuropathy
Germ cell tumor
Global cerebellar malformation
Glycogen storage disease
Hemophagocytic syndrome
Adolescent, Childhood, Infancy
Hereditary ataxia
Hereditary episodic ataxia
Histiocytic and dendritic cell tumor
Human prion disease
Adult
Idiopathic inflammatory myopathy
Indolent B-cell non-Hodgkin lymphoma
Adult
Inherited epidermolysis bullosa
Autosomal dominant, Autosomal recessive
All ages
Inherited ichthyosis
Inherited ichthyosis syndromic form
Inherited non-syndromic ichthyosis
Interstitial lung disease
Intractable diarrhea of infancy
Childhood
Isolated rare lymphatic malformation
Not applicable
Infancy, Neonatal
Jejunal neuroendocrine tumor
Adult
Joubert syndrome and related disorders
Autosomal recessive, X-linked recessive
Infancy, Neonatal