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

Gallbladder neuroendocrine tumor

ORPHA:100086Kr.

Gamma-aminobutyric acid transaminase deficiency

ORPHA:2066Kr.
Autosomal recessive

Gamma-glutamyl transpeptidase deficiency

ORPHA:33573Kr.
Autosomal recessive

Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5

ORPHA:353Kr.
Autosomal recessive

Gangliocytoma

ORPHA:251937Kr.

Ganglioneuroblastoma

ORPHA:251877Kr.
Not applicable

Ganglioneuroma

ORPHA:251992Kr.

Gastric adenocarcinoma and proximal polyposis of the stomach

ORPHA:314022Kr.
Autosomal dominant

Gastric linitis plastica

ORPHA:36273Kr.

Gastrocutaneous syndrome

ORPHA:2069Kr.

Gastrointestinal stromal tumor

ORPHA:44890Kr.
Autosomal dominant, Not applicable

Gaucher disease

ORPHA:355Kr.
Autosomal recessive

Gelatinous drop-like corneal dystrophy

ORPHA:98957Kr.
Autosomal recessive

Generalized arterial calcification of infancy

ORPHA:51608Kr.
Autosomal dominant, Autosomal recessive

Generalized basaloid follicular hamartoma syndrome

ORPHA:168632Kr.
Autosomal dominant

Generalized epilepsy-paroxysmal dyskinesia syndrome

ORPHA:79137Kr.
Autosomal dominant

Generalized eruptive histiocytosis

ORPHA:157991Kr.
Not applicable

Generalized eruptive keratoacanthoma

ORPHA:411777Kr.
Not applicable

Generalized essential telangiectasia

ORPHA:280774Kr.
Not applicable

Generalized glucocorticoid resistance syndrome

ORPHA:786Kr.
Autosomal dominant, Autosomal recessive, Not applicable

Generalized peeling skin syndrome

ORPHA:263543Kr.
Autosomal recessive

Generalized pustular psoriasis

ORPHA:247353Kr.
Autosomal recessive, Not applicable

Genetic central precocious puberty in female

ORPHA:650077Kr.

Genetic epilepsy with febrile seizure plus

ORPHA:36387Kr.
Autosomal dominant