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
Fever-associated acute infantile liver failure syndrome
Autosomal recessive
Infancy
Fibrillary astrocytoma
Fibroblastic rheumatism
Adolescent, Adult, Childhood
Fibrochondrogenesis
Autosomal dominant, Autosomal recessive
Neonatal
Fibrodysplasia ossificans progressiva
Autosomal dominant, Not applicable
Childhood
Fibrohistiocytic inflammatory pseudotumor of the liver
Adult, Elderly
Fibrolamellar hepatocellular carcinoma
Not applicable
Adolescent, Adult
Fibromuscular dysplasia of the arteries of the extremities
Not applicable
Fibromuscular dysplasia of the cervical and intracranial arteries
Not applicable
Fibromuscular dysplasia of the coronary arteries
Not applicable
Fibromuscular dysplasia of the renal arteries
Not applicable
Fibromuscular dysplasia of the visceral arteries
Not applicable
Fibronectin glomerulopathy
Autosomal dominant
All ages
Fibrosarcoma
Not applicable
All ages
Fibrosis-neurodegeneration-cerebral angiomatosis syndrome
Infancy, Neonatal
Fibrotic hypersensitivity pneumonitis
Not applicable
Fibrous dysplasia of bone
Not applicable
Adolescent, Adult, Childhood
Fibular aplasia-complex brachydactyly syndrome
Autosomal recessive
Antenatal, Neonatal
Fibular aplasia-ectrodactyly syndrome
Autosomal dominant
Neonatal
Fibular dimelia-diplopodia syndrome
Not applicable
Neonatal
Fibulo-ulnar hypoplasia-renal anomalies syndrome
Antenatal, Neonatal
Filariasis
Not applicable
All ages
Filippi syndrome
Autosomal recessive
Infancy, Neonatal
Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome
Infancy, Neonatal