Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Gastrointestinal stromal tumor
Autosomal dominant, Not applicable
Adolescent, Adult, Childhood
Gastrointestinal tract arteriovenous malformation
Not applicable
Gastroschisis
Not applicable
Antenatal
Gaucher disease
Autosomal recessive
All ages
Gaucher disease type 1
Autosomal recessive
All ages
Gaucher disease type 2
Autosomal recessive
Infancy
Gaucher disease type 3
Autosomal recessive
All ages
Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
Autosomal recessive
Childhood
Gelatinous drop-like corneal dystrophy
Autosomal recessive
Childhood
Geleophysic dysplasia
Autosomal dominant, Autosomal recessive
Childhood
Gemignani syndrome
Autosomal recessive
Adult
Gemistocytic astrocytoma
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 galactose epimerase deficiency
Autosomal recessive
Generalized glucocorticoid resistance syndrome
Autosomal dominant, Autosomal recessive, Not applicable
All ages
Generalized juvenile polyposis/juvenile polyposis coli
Autosomal dominant
All ages
Generalized peeling skin syndrome
Autosomal recessive
Infancy, Neonatal
Generalized pseudohypoaldosteronism type 1
Autosomal recessive
Infancy, Neonatal
Generalized pustular psoriasis
Autosomal recessive, Not applicable
Adult