Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Gray platelet syndrome
Autosomal dominant, Autosomal recessive
Childhood
Grayson-Wilbrandt corneal dystrophy
Autosomal dominant
Adolescent, Adult, Childhood
Greenberg dysplasia
Autosomal recessive
Antenatal, Neonatal
Greig cephalopolysyndactyly syndrome
Autosomal dominant
Antenatal
Greig cephalopolysyndactyly-contiguous gene syndrome
Antenatal
Griscelli syndrome
Autosomal recessive
Childhood, Infancy
Griscelli syndrome type 1
Autosomal recessive
Childhood, Infancy
Griscelli syndrome type 2
Autosomal recessive
Childhood, Infancy
Griscelli syndrome type 3
Autosomal recessive
Childhood
Grisel syndrome
Not applicable
Childhood
Growing teratoma syndrome
Not applicable
Adult
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-hydrocephaly-lung hypoplasia syndrome
Antenatal
Growth delay-intellectual disability-hepatopathy syndrome
Autosomal recessive
Infancy, Neonatal
Growth retardation-mild developmental delay-chronic hepatitis syndrome
Autosomal recessive
Infancy, Neonatal
Grubben-de Cock-Borghgraef syndrome
Antenatal, Neonatal
Guanidinoacetate methyltransferase deficiency
Autosomal recessive
Childhood, Infancy
Guillain-Barré syndrome
Multigenic/multifactorial
All ages
Guttmacher syndrome
Autosomal dominant
Infancy, Neonatal
Gynandroblastoma
Gyrate atrophy of choroid and retina
Autosomal recessive
Childhood
Gómez-López-Hernández syndrome
Not applicable
Neonatal