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
Pulmonary fungal infections in patients deemed at risk
Not applicable
All ages
Recurrent hepatitis C virus induced liver disease in liver transplant recipients
Not applicable
All ages
Sagliker syndrome
Multigenic/multifactorial
All ages
Scarring in glaucoma filtration surgical procedures
Not applicable
All ages
Sepsis in premature infants
Not applicable
Neonatal
Spinal cord injury
Not applicable
All ages
Sudden sensorineural hearing loss
Not applicable
All ages
Sydenham chorea
Adolescent, Adult, Childhood
Transient hyperammonemia of the newborn
Neonatal
Uremic pruritus
Not applicable
Adolescent, Adult, Childhood, Elderly
Ventilator-induced diaphragmatic dysfunction
All ages
Zinc-responsive necrolytic acral erythema
Not applicable
All ages