Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Gallbladder neuroendocrine tumor
Adult
Gamma-aminobutyric acid transaminase deficiency
Autosomal recessive
Infancy, Neonatal
Gamma-glutamyl transpeptidase deficiency
Autosomal recessive
Infancy
Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5
Autosomal recessive
Childhood
Gangliocytoma
Adolescent, Childhood, Infancy
Ganglioneuroblastoma
Not applicable
Childhood, Infancy
Ganglioneuroma
Adolescent, Childhood, Infancy
Gastric adenocarcinoma and proximal polyposis of the stomach
Autosomal dominant
Adult
Gastric linitis plastica
Adult
Gastrocutaneous syndrome
Adolescent, Adult
Gastrointestinal stromal tumor
Autosomal dominant, Not applicable
Adolescent, Adult, Childhood
Gaucher disease
Autosomal recessive
All ages
Gelatinous drop-like corneal dystrophy
Autosomal recessive
Childhood
Generalized arterial calcification of infancy
Autosomal dominant, Autosomal recessive
Antenatal, Infancy, Neonatal
Generalized basaloid follicular hamartoma syndrome
Autosomal dominant
Generalized epilepsy-paroxysmal dyskinesia syndrome
Autosomal dominant
Childhood
Generalized eruptive histiocytosis
Not applicable
Adolescent, Adult, Childhood, Elderly
Generalized eruptive keratoacanthoma
Not applicable
Adult, Elderly
Generalized essential telangiectasia
Not applicable
Adolescent, Adult
Generalized glucocorticoid resistance syndrome
Autosomal dominant, Autosomal recessive, Not applicable
All ages
Generalized peeling skin syndrome
Autosomal recessive
Infancy, Neonatal
Generalized pustular psoriasis
Autosomal recessive, Not applicable
Adult
Genetic central precocious puberty in female
Genetic epilepsy with febrile seizure plus
Autosomal dominant
Childhood