MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 3,968 заболеваний (Ауру) Қалпына келтіру

Gonadoblastoma

ORPHA:206484Ауру

Gonococcal conjunctivitis

ORPHA:1482Ауру

Graft versus host disease

ORPHA:39812Ауру
Not applicable

Graham Little-Piccardi-Lassueur syndrome

ORPHA:505Ауру

Granular corneal dystrophy type I

ORPHA:98962Ауру
Autosomal dominant

Granular corneal dystrophy type II

ORPHA:98963Ауру
Autosomal dominant

Granulomatosis with polyangiitis

ORPHA:900Ауру
Not applicable

Granulomatous mastitis

ORPHA:64722Ауру

Granulomatous slack skin

ORPHA:33111Ауру
Not applicable

Gray platelet syndrome

ORPHA:721Ауру
Autosomal dominant, Autosomal recessive

Grayson-Wilbrandt corneal dystrophy

ORPHA:293375Ауру
Autosomal dominant

Greenberg dysplasia

ORPHA:1426Ауру
Autosomal recessive

Griscelli syndrome

ORPHA:381Ауру
Autosomal recessive

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

ORPHA:391348Ауру
Autosomal recessive

Growth delay due to insulin-like growth factor I resistance

ORPHA:73273Ауру
Autosomal dominant, Autosomal recessive

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

ORPHA:73272Ауру
Autosomal recessive

Growth delay-intellectual disability-hepatopathy syndrome

ORPHA:541423Ауру
Autosomal recessive

Growth retardation-mild developmental delay-chronic hepatitis syndrome

ORPHA:391366Ауру
Autosomal recessive

Guanidinoacetate methyltransferase deficiency

ORPHA:382Ауру
Autosomal recessive

Gynandroblastoma

ORPHA:99914Ауру

Gyrate atrophy of choroid and retina

ORPHA:414Ауру
Autosomal recessive

HANAC syndrome

ORPHA:73229Ауру
Autosomal dominant

HELLP syndrome

ORPHA:244242Ауру
Multigenic/multifactorial

HJV or HAMP-related hemochromatosis

ORPHA:79230Ауру
Autosomal recessive