MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Fingerprint body myopathy

ORPHA:97232Kr.

Fish-eye disease

ORPHA:79292Kl. subt.
Autosomal recessive

Fixed drug eruption

ORPHA:293812Kr.
Not applicable

Fixed subaortic stenosis

ORPHA:3092Morph.
No data available

Flat face-microstomia-ear anomaly syndrome

ORPHA:1968Malf.
Unknown

Fleck corneal dystrophy

ORPHA:98970Kr.
Autosomal dominant

Floating-Harbor syndrome

ORPHA:2044Malf.
Autosomal dominant

Florid cemento-osseous dysplasia

ORPHA:83451Kr.
Not applicable

Flynn-Aird syndrome

ORPHA:2047Kr.
Autosomal dominant

Focal dermal hypoplasia

ORPHA:2092Malf.
X-linked dominant

Focal epilepsy-intellectual disability-cerebro-cerebellar malformation

ORPHA:352587Kr.
Autosomal recessive

Focal facial dermal dysplasia

ORPHA:398166Malf.
Autosomal dominant, Autosomal recessive

Focal facial dermal dysplasia type I

ORPHA:79133Kl. subt.
Autosomal dominant

Focal facial dermal dysplasia type II

ORPHA:398173Kl. subt.
Autosomal dominant

Focal facial dermal dysplasia type III

ORPHA:1807Kl. subt.
Autosomal dominant, Autosomal recessive

Focal facial dermal dysplasia type IV

ORPHA:398189Kl. subt.
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

Focal stiff limb syndrome

ORPHA:443804Kl. subt.
Not applicable

Focal, segmental or multifocal dystonia

ORPHA:1866Kat.
Autosomal dominant

Foix-Chavany-Marie syndrome

ORPHA:2048Malf.
Not applicable

Folinic acid-responsive seizures

ORPHA:79097Kr.
Unknown

Follicular cholangitis and pancreatitis

ORPHA:300552Kr.
Unknown