MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Female infertility due to zona pellucida defect

ORPHA:404466Kr.
Autosomal dominant, Autosomal recessive

Ferro-cerebro-cutaneous syndrome

ORPHA:397922Kr.
X-linked recessive

Ferroportin disease

ORPHA:648562Kr.

Fetal akinesia-cerebral and retinal hemorrhage syndrome

ORPHA:363409Kr.
Autosomal recessive

Fetal and neonatal alloimmune thrombocytopenia

ORPHA:853Kr.
Not applicable

Fetal cytomegalovirus syndrome

ORPHA:294Kr.
Not applicable

Fever-associated acute infantile liver failure syndrome

ORPHA:464724Kr.
Autosomal recessive

Fibroblastic rheumatism

ORPHA:477650Kr.

Fibrochondrogenesis

ORPHA:2021Kr.
Autosomal dominant, Autosomal recessive

Fibrodysplasia ossificans progressiva

ORPHA:337Kr.
Autosomal dominant, Not applicable

Fibrolamellar hepatocellular carcinoma

ORPHA:401920Kr.
Not applicable

Fibronectin glomerulopathy

ORPHA:84090Kr.
Autosomal dominant

Fibrosarcoma

ORPHA:2030Kr.
Not applicable

Fibrosis-neurodegeneration-cerebral angiomatosis syndrome

ORPHA:621758Kr.

Fingerprint body myopathy

ORPHA:97232Kr.

Fixed drug eruption

ORPHA:293812Kr.
Not applicable

Fleck corneal dystrophy

ORPHA:98970Kr.
Autosomal dominant

Florid cemento-osseous dysplasia

ORPHA:83451Kr.
Not applicable

Flynn-Aird syndrome

ORPHA:2047Kr.
Autosomal dominant

Focal epilepsy-intellectual disability-cerebro-cerebellar malformation

ORPHA:352587Kr.
Autosomal recessive

Focal myositis

ORPHA:48918Kr.
Not applicable

Focal palmoplantar and gingival keratoderma

ORPHA:2200Kr.

Focal palmoplantar keratoderma with joint keratoses

ORPHA:370002Kr.
Autosomal dominant

Folinic acid-responsive seizures

ORPHA:79097Kr.
Unknown