MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов
Найдено 3,968 заболеваний (Заболевание)Сбросить

Gallbladder neuroendocrine tumor

ORPHA:100086Заболевание

Gamma-aminobutyric acid transaminase deficiency

ORPHA:2066Заболевание
Autosomal recessive

Gamma-glutamyl transpeptidase deficiency

ORPHA:33573Заболевание
Autosomal recessive

Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5

ORPHA:353Заболевание
Autosomal recessive

Gangliocytoma

ORPHA:251937Заболевание

Ganglioneuroblastoma

ORPHA:251877Заболевание
Not applicable

Ganglioneuroma

ORPHA:251992Заболевание

Gastric adenocarcinoma and proximal polyposis of the stomach

ORPHA:314022Заболевание
Autosomal dominant

Gastric linitis plastica

ORPHA:36273Заболевание

Gastrocutaneous syndrome

ORPHA:2069Заболевание

Gastrointestinal stromal tumor

ORPHA:44890Заболевание
Autosomal dominant, Not applicable

Gaucher disease

ORPHA:355Заболевание
Autosomal recessive

Gelatinous drop-like corneal dystrophy

ORPHA:98957Заболевание
Autosomal recessive

Generalized arterial calcification of infancy

ORPHA:51608Заболевание
Autosomal dominant, Autosomal recessive

Generalized basaloid follicular hamartoma syndrome

ORPHA:168632Заболевание
Autosomal dominant

Generalized epilepsy-paroxysmal dyskinesia syndrome

ORPHA:79137Заболевание
Autosomal dominant

Generalized eruptive histiocytosis

ORPHA:157991Заболевание
Not applicable

Generalized eruptive keratoacanthoma

ORPHA:411777Заболевание
Not applicable

Generalized essential telangiectasia

ORPHA:280774Заболевание
Not applicable

Generalized glucocorticoid resistance syndrome

ORPHA:786Заболевание
Autosomal dominant, Autosomal recessive, Not applicable

Generalized peeling skin syndrome

ORPHA:263543Заболевание
Autosomal recessive

Generalized pustular psoriasis

ORPHA:247353Заболевание
Autosomal recessive, Not applicable

Genetic central precocious puberty in female

ORPHA:650077Заболевание

Genetic epilepsy with febrile seizure plus

ORPHA:36387Заболевание
Autosomal dominant