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
Idiopathic eosinophilic myositis
Not applicable
Idiopathic gastroparesis
Adolescent, Adult, Childhood, Elderly, Infancy
Idiopathic giant cell myocarditis
Adolescent, Adult, Childhood, Infancy
Idiopathic hypercalciuria
Autosomal dominant
Adolescent, Adult, Childhood
Idiopathic hypereosinophilic syndrome
Not applicable
Adult
Idiopathic hypersomnia
Unknown
All ages
Idiopathic inflammatory myopathy
Idiopathic intracranial hypertension
Not applicable
Adult, Elderly
Idiopathic isolated micropenis
Neonatal
Idiopathic juvenile osteoporosis
Multigenic/multifactorial, Not applicable
Adolescent, Childhood
Idiopathic linear interstitial keratitis
Unknown
Adult
Idiopathic localized lipodystrophy
Adolescent, Adult, Childhood, Infancy
Idiopathic macular telangiectasia type 1
Adult
Idiopathic macular telangiectasia type 3
Adult
Idiopathic multicentric Castleman disease
All ages
Idiopathic multidrug-resistant nephrotic syndrome
All ages
Idiopathic neonatal atrial flutter
Not applicable
Infancy, Neonatal
Idiopathic nephrotic syndrome
All ages
Idiopathic non-lupus full-house nephropathy
All ages
Idiopathic panuveitis
Not applicable
Adolescent, Adult, Childhood, Elderly
Idiopathic peliosis hepatis
Adult, Childhood
Idiopathic phalangeal acro-osteolysis
Not applicable
Idiopathic pleuroparenchymal fibroelastosis
Adolescent, Adult, Elderly
Idiopathic pulmonary arterial hypertension
Not applicable
All ages