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
Macrophage activation syndrome
Adolescent, Adult, Childhood
Mal de débarquement
Not applicable
All ages
Meigs syndrome
Not applicable
Adult
Mirizzi syndrome
Adult, Elderly
Mounier-Kühn syndrome
Not applicable
All ages
Nelson syndrome
Adult, Elderly
Neonatal compartment syndrome
Neonatal
Nicolau syndrome
Non-malignant and non-cirrhotic portal vein thrombosis
Not applicable
All ages
Painful legs and moving toes syndrome
Adult
Pediatric arterial ischemic stroke
Not applicable
Adolescent, Childhood, Infancy, Neonatal
Placental insufficiency
Not applicable
Adult
Polyclonal hyperviscosity syndrome
Not applicable
Adolescent, Adult, All ages, Elderly
Postorgasmic illness syndrome
Not applicable
Adolescent, Adult
Primary progressive freezing gait
Unknown
Adult
Pseudo-Meigs syndrome
Not applicable
Adult
Psychogenic movement disorders
Not applicable
Adolescent, Adult, Childhood, Elderly
Reversible cerebral vasoconstriction syndrome
Not applicable
Adult
Semicircular canal dehiscence syndrome
Not applicable
All ages
Spasmus nutans
Unknown
Infancy
Spastic paraparesis-cataracts-speech delay syndrome
Autosomal dominant
Spastic paraplegia-nephritis-deafness syndrome
Autosomal dominant
No data available
TEMPI syndrome
Adult