Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Genetic central precocious puberty in female
Genetic central precocious puberty in male
Genetic congenital malformation of the eye with glaucoma as a major feature
Neonatal
Genetic epilepsy with febrile seizure plus
Autosomal dominant
Childhood
Genetic hyperferritinemia without iron overload
Autosomal dominant, Autosomal recessive
No data available
Genetic non-syndromic obesity
Not applicable
Childhood, Infancy
Genetic peripheral neuropathy
Genetic recurrent myoglobinuria
Autosomal dominant, Autosomal recessive, Not applicable
Childhood
Genetic transient congenital hypothyroidism
Autosomal recessive
Infancy, Neonatal
Genitopalatocardiac syndrome
Antenatal, Neonatal
Genitopatellar syndrome
Autosomal dominant, Autosomal recessive
Childhood
Genochondromatosis type 1
Autosomal dominant
Childhood
Genochondromatosis type 2
Childhood
Germ cell tumor
German syndrome
Autosomal recessive
Neonatal
Germinoma of the central nervous system
Not applicable
Adolescent, Adult, Childhood
Geroderma osteodysplastica
Autosomal recessive
Neonatal
Gerstmann-Straussler-Scheinker syndrome
Autosomal dominant, Not applicable
Adult
Gestational choriocarcinoma
Not applicable
Adult
Gestational trophoblastic neoplasm
Not applicable
Adult
Ghosal hematodiaphyseal dysplasia
Autosomal recessive
Infancy, Neonatal
Giant axonal neuropathy
Autosomal recessive
Childhood, Infancy
Giant cell arteritis
Multigenic/multifactorial
Adult
Giant cell glioblastoma
Not applicable
Adult