Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Gonadoblastoma
Adolescent
Gonococcal conjunctivitis
All ages
Graft versus host disease
Not applicable
All ages
Graham Little-Piccardi-Lassueur syndrome
Adult
Granular corneal dystrophy type I
Autosomal dominant
Childhood
Granular corneal dystrophy type II
Autosomal dominant
Childhood
Granulomatosis with polyangiitis
Not applicable
Adolescent, Adult, Childhood, Elderly
Granulomatous mastitis
Adolescent, Adult, Elderly
Granulomatous slack skin
Not applicable
Adult
Gray platelet syndrome
Autosomal dominant, Autosomal recessive
Childhood
Grayson-Wilbrandt corneal dystrophy
Autosomal dominant
Adolescent, Adult, Childhood
Greenberg dysplasia
Autosomal recessive
Antenatal, Neonatal
Griscelli syndrome
Autosomal recessive
Childhood, Infancy
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
Autosomal recessive
Infancy, Neonatal
Growth delay due to insulin-like growth factor I resistance
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Growth delay due to insulin-like growth factor type 1 deficiency
Autosomal recessive
Antenatal, Infancy, Neonatal
Growth delay-intellectual disability-hepatopathy syndrome
Autosomal recessive
Infancy, Neonatal
Growth retardation-mild developmental delay-chronic hepatitis syndrome
Autosomal recessive
Infancy, Neonatal
Guanidinoacetate methyltransferase deficiency
Autosomal recessive
Childhood, Infancy
Gynandroblastoma
Gyrate atrophy of choroid and retina
Autosomal recessive
Childhood
HANAC syndrome
Autosomal dominant
Childhood
HELLP syndrome
Multigenic/multifactorial
Adult
HJV or HAMP-related hemochromatosis
Autosomal recessive
Adolescent, Adult, Childhood