MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Gray platelet syndrome

ORPHA:721Заболевание
Autosomal dominant, Autosomal recessive

Grayson-Wilbrandt corneal dystrophy

ORPHA:293375Заболевание
Autosomal dominant

Greenberg dysplasia

ORPHA:1426Заболевание
Autosomal recessive

Greig cephalopolysyndactyly syndrome

ORPHA:380Мальформация
Autosomal dominant

Greig cephalopolysyndactyly-contiguous gene syndrome

ORPHA:658805Мальформация

Griscelli syndrome

ORPHA:381Заболевание
Autosomal recessive

Griscelli syndrome type 1

ORPHA:79476Клин. подтип
Autosomal recessive

Griscelli syndrome type 2

ORPHA:79477Клин. подтип
Autosomal recessive

Griscelli syndrome type 3

ORPHA:79478Клин. подтип
Autosomal recessive

Grisel syndrome

ORPHA:662255Clinical syndrome
Not applicable

Growing teratoma syndrome

ORPHA:314613Особая клин. ситуация
Not applicable

Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome

ORPHA:391348Заболевание
Autosomal recessive

Growth delay due to insulin-like growth factor I resistance

ORPHA:73273Заболевание
Autosomal dominant, Autosomal recessive

Growth delay due to insulin-like growth factor type 1 deficiency

ORPHA:73272Заболевание
Autosomal recessive

Growth delay-hydrocephaly-lung hypoplasia syndrome

ORPHA:3035Мальформация

Growth delay-intellectual disability-hepatopathy syndrome

ORPHA:541423Заболевание
Autosomal recessive

Growth retardation-mild developmental delay-chronic hepatitis syndrome

ORPHA:391366Заболевание
Autosomal recessive

Grubben-de Cock-Borghgraef syndrome

ORPHA:2101Мальформация

Guanidinoacetate methyltransferase deficiency

ORPHA:382Заболевание
Autosomal recessive

Guillain-Barré syndrome

ORPHA:2103Клин. группа
Multigenic/multifactorial

Guttmacher syndrome

ORPHA:2957Мальформация
Autosomal dominant

Gynandroblastoma

ORPHA:99914Заболевание

Gyrate atrophy of choroid and retina

ORPHA:414Заболевание
Autosomal recessive

Gómez-López-Hernández syndrome

ORPHA:1532Мальформация
Not applicable