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
Beta-mercaptolactate cysteine disulfiduria
No data available
Carnosinase deficiency
Autosomal recessive
Infancy
Congenital deficiency in alpha-fetoprotein
Autosomal recessive
Antenatal, Neonatal
Familial Hyperalphalipoproteinemia
Autosomal dominant
Genetic hyperferritinemia without iron overload
Autosomal dominant, Autosomal recessive
No data available
Hereditary persistence of alpha-fetoprotein
Autosomal dominant
Adolescent
Idiopathic CD4 lymphocytopenia
Not applicable
Adult
Isolated asymptomatic elevation of creatine phosphokinase
Autosomal dominant
All ages
L-ferritin deficiency
Autosomal dominant, Autosomal recessive
Childhood
Lipoyl transferase 2 deficiency
No data available
No data available
Methylmalonic aciduria due to transcobalamin receptor defect
Autosomal recessive
Infancy, Neonatal