MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Fever-associated acute infantile liver failure syndrome

ORPHA:464724Kr.
Autosomal recessive

Fibrillary astrocytoma

ORPHA:251601His. subt.

Fibroblastic rheumatism

ORPHA:477650Kr.

Fibrochondrogenesis

ORPHA:2021Kr.
Autosomal dominant, Autosomal recessive

Fibrodysplasia ossificans progressiva

ORPHA:337Kr.
Autosomal dominant, Not applicable

Fibrohistiocytic inflammatory pseudotumor of the liver

ORPHA:555434Kl. subt.

Fibrolamellar hepatocellular carcinoma

ORPHA:401920Kr.
Not applicable

Fibromuscular dysplasia of the arteries of the extremities

ORPHA:698069Kl. subt.
Not applicable

Fibromuscular dysplasia of the cervical and intracranial arteries

ORPHA:698036Kl. subt.
Not applicable

Fibromuscular dysplasia of the coronary arteries

ORPHA:698059Kl. subt.
Not applicable

Fibromuscular dysplasia of the renal arteries

ORPHA:698043Kl. subt.
Not applicable

Fibromuscular dysplasia of the visceral arteries

ORPHA:698063Kl. subt.
Not applicable

Fibronectin glomerulopathy

ORPHA:84090Kr.
Autosomal dominant

Fibrosarcoma

ORPHA:2030Kr.
Not applicable

Fibrosis-neurodegeneration-cerebral angiomatosis syndrome

ORPHA:621758Kr.

Fibrotic hypersensitivity pneumonitis

ORPHA:686465Kl. subt.
Not applicable

Fibrous dysplasia of bone

ORPHA:249Malf.
Not applicable

Fibular aplasia-complex brachydactyly syndrome

ORPHA:2639Malf.
Autosomal recessive

Fibular aplasia-ectrodactyly syndrome

ORPHA:1118Malf.
Autosomal dominant

Fibular dimelia-diplopodia syndrome

ORPHA:1757Malf.
Not applicable

Fibulo-ulnar hypoplasia-renal anomalies syndrome

ORPHA:2256Malf.

Filariasis

ORPHA:2034Kat.
Not applicable

Filippi syndrome

ORPHA:3255Malf.
Autosomal recessive

Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome

ORPHA:369979Malf.