Orphanet Datenbank · Orphadata CC-BY-4.0
Seltene Erkrankungen (Orphan)
Komplette Bibliothek mit 7,547 Erkrankungen — Genetik, Phänotypen, Epidemiologie, Orphan-Arzneimittel und Studien.
7,547
Erkrankungen
4,552
Gene
8,700
Phänotypen
140
Regionen
Alle (7,547)Bio-AnomalieKategorieKlinische GruppeKlinischer SubtypClinical syndromeErkrankungÄtiologischer SubtypHistopathologischer SubtypMalformationssyndromMorphologische AnomalieBesondere klinische 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