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 pulmonary fibrosis
Multigenic/multifactorial
Adult
Idiopathic pulmonary hemosiderosis
Childhood
Idiopathic recurrent pericarditis
Not applicable
All ages
Idiopathic recurrent stupor
Not applicable
Adult
Idiopathic spontaneous coronary artery dissection
Not applicable
Adult
Idiopathic steroid-resistant nephrotic syndrome
Adolescent, Adult, Childhood
Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy
All ages
Idiopathic steroid-sensitive nephrotic syndrome
Unknown
All ages
Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance
All ages
Idiopathic trachyonychia
Autosomal dominant
Childhood
Idiopathic triglyceride deposit cardiomyovasculopathy
Unknown
Idiopathic uveal effusion syndrome
Unknown
Adult
Idiopathic ventricular fibrillation
Autosomal dominant, Not applicable
All ages
Idiopathic/heritable pulmonary arterial hypertension
Autosomal dominant, Autosomal recessive, Not applicable
All ages
IgA pemphigus
All ages
IgG4-related aortitis
Not applicable
Adult, Elderly
IgG4-related dacryoadenitis and sialadenitis
Not applicable
All ages
IgG4-related disease
Not applicable
Adult
IgG4-related kidney disease
Not applicable
Adult, Elderly
IgG4-related mediastinitis
Not applicable
IgG4-related mesenteritis
Not applicable
Adult
IgG4-related ophthalmic disease
Not applicable
Adult, Elderly
IgG4-related pachymeningitis
Not applicable
Adult, Elderly
IgG4-related retroperitoneal fibrosis
Not applicable, Unknown
Adult