MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Gastrointestinal stromal tumor

ORPHA:44890Kr.
Autosomal dominant, Not applicable

Gastrointestinal tract arteriovenous malformation

ORPHA:693832Malf.
Not applicable

Gastroschisis

ORPHA:2368Morph.
Not applicable

Gaucher disease

ORPHA:355Kr.
Autosomal recessive

Gaucher disease type 1

ORPHA:77259Kl. subt.
Autosomal recessive

Gaucher disease type 2

ORPHA:77260Kl. subt.
Autosomal recessive

Gaucher disease type 3

ORPHA:77261Kl. subt.
Autosomal recessive

Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome

ORPHA:2072Kl. subt.
Autosomal recessive

Gelatinous drop-like corneal dystrophy

ORPHA:98957Kr.
Autosomal recessive

Geleophysic dysplasia

ORPHA:2623Malf.
Autosomal dominant, Autosomal recessive

Gemignani syndrome

ORPHA:2074Malf.
Autosomal recessive

Gemistocytic astrocytoma

ORPHA:251604His. subt.

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 galactose epimerase deficiency

ORPHA:308487Kl. subt.
Autosomal recessive

Generalized glucocorticoid resistance syndrome

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

Generalized juvenile polyposis/juvenile polyposis coli

ORPHA:329971Kl. subt.
Autosomal dominant

Generalized peeling skin syndrome

ORPHA:263543Kr.
Autosomal recessive

Generalized pseudohypoaldosteronism type 1

ORPHA:171876Kl. subt.
Autosomal recessive

Generalized pustular psoriasis

ORPHA:247353Kr.
Autosomal recessive, Not applicable