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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Gray platelet syndrome

ORPHA:721Disease
Autosomal dominant, Autosomal recessive

Grayson-Wilbrandt corneal dystrophy

ORPHA:293375Disease
Autosomal dominant

Greenberg dysplasia

ORPHA:1426Disease
Autosomal recessive

Greig cephalopolysyndactyly syndrome

ORPHA:380Malform.
Autosomal dominant

Greig cephalopolysyndactyly-contiguous gene syndrome

ORPHA:658805Malform.

Griscelli syndrome

ORPHA:381Disease
Autosomal recessive

Griscelli syndrome type 1

ORPHA:79476Clin. sub.
Autosomal recessive

Griscelli syndrome type 2

ORPHA:79477Clin. sub.
Autosomal recessive

Griscelli syndrome type 3

ORPHA:79478Clin. sub.
Autosomal recessive

Grisel syndrome

ORPHA:662255Clinical syndrome
Not applicable

Growing teratoma syndrome

ORPHA:314613Situation
Not applicable

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

ORPHA:391348Disease
Autosomal recessive

Growth delay due to insulin-like growth factor I resistance

ORPHA:73273Disease
Autosomal dominant, Autosomal recessive

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

ORPHA:73272Disease
Autosomal recessive

Growth delay-hydrocephaly-lung hypoplasia syndrome

ORPHA:3035Malform.

Growth delay-intellectual disability-hepatopathy syndrome

ORPHA:541423Disease
Autosomal recessive

Growth retardation-mild developmental delay-chronic hepatitis syndrome

ORPHA:391366Disease
Autosomal recessive

Grubben-de Cock-Borghgraef syndrome

ORPHA:2101Malform.

Guanidinoacetate methyltransferase deficiency

ORPHA:382Disease
Autosomal recessive

Guillain-Barré syndrome

ORPHA:2103Clin. grp.
Multigenic/multifactorial

Guttmacher syndrome

ORPHA:2957Malform.
Autosomal dominant

Gynandroblastoma

ORPHA:99914Disease

Gyrate atrophy of choroid and retina

ORPHA:414Disease
Autosomal recessive

Gómez-López-Hernández syndrome

ORPHA:1532Malform.
Not applicable