MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Genetic central precocious puberty in female

ORPHA:650077Заболевание

Genetic central precocious puberty in male

ORPHA:650097Клин. подтип

Genetic congenital malformation of the eye with glaucoma as a major feature

ORPHA:525677Категория

Genetic epilepsy with febrile seizure plus

ORPHA:36387Заболевание
Autosomal dominant

Genetic hyperferritinemia without iron overload

ORPHA:254704Биоаномалия
Autosomal dominant, Autosomal recessive

Genetic non-syndromic obesity

ORPHA:98267Заболевание
Not applicable

Genetic peripheral neuropathy

ORPHA:98497Категория

Genetic recurrent myoglobinuria

ORPHA:99845Заболевание
Autosomal dominant, Autosomal recessive, Not applicable

Genetic transient congenital hypothyroidism

ORPHA:226316Заболевание
Autosomal recessive

Genitopalatocardiac syndrome

ORPHA:2075Мальформация

Genitopatellar syndrome

ORPHA:85201Мальформация
Autosomal dominant, Autosomal recessive

Genochondromatosis type 1

ORPHA:85197Заболевание
Autosomal dominant

Genochondromatosis type 2

ORPHA:93398Заболевание

Germ cell tumor

ORPHA:3399Категория

German syndrome

ORPHA:2077Мальформация
Autosomal recessive

Germinoma of the central nervous system

ORPHA:91352Клин. подтип
Not applicable

Geroderma osteodysplastica

ORPHA:2078Мальформация
Autosomal recessive

Gerstmann-Straussler-Scheinker syndrome

ORPHA:356Заболевание
Autosomal dominant, Not applicable

Gestational choriocarcinoma

ORPHA:99926Заболевание
Not applicable

Gestational trophoblastic neoplasm

ORPHA:59305Клин. группа
Not applicable

Ghosal hematodiaphyseal dysplasia

ORPHA:1802Мальформация
Autosomal recessive

Giant axonal neuropathy

ORPHA:643Заболевание
Autosomal recessive

Giant cell arteritis

ORPHA:397Заболевание
Multigenic/multifactorial

Giant cell glioblastoma

ORPHA:251579Гист. подтип
Not applicable