Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
GNE myopathy
Autosomal dominant, Autosomal recessive
Adolescent, Adult
GRACILE syndrome
Autosomal recessive
Antenatal, Neonatal
GRFoma
Not applicable
Adult
GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
Autosomal dominant
Childhood, Infancy, Neonatal
GTP cyclohydrolase I deficiency
Autosomal recessive
Infancy, Neonatal
Gabriele-de Vries syndrome
Autosomal dominant
Antenatal, Neonatal
Gaisböck syndrome
Adult
Galactokinase deficiency
Autosomal recessive
Infancy, Neonatal
Galactose epimerase deficiency
Autosomal recessive
Infancy, Neonatal
Galactose mutarotase deficiency
Autosomal recessive
Infancy, Neonatal
Galactosemia
Autosomal recessive
Childhood, Infancy, Neonatal
Galactosialidosis
Autosomal recessive
All ages
Gallbladder neuroendocrine tumor
Adult
Galloway-Mowat syndrome
Autosomal recessive, X-linked recessive
Childhood, Infancy, Neonatal
Gamma-aminobutyric acid transaminase deficiency
Autosomal recessive
Infancy, Neonatal
Gamma-glutamyl transpeptidase deficiency
Autosomal recessive
Infancy
Gamma-heavy chain disease
Adult
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