MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Gonadoblastoma

ORPHA:206484Disease

Gonococcal conjunctivitis

ORPHA:1482Disease

Graft versus host disease

ORPHA:39812Disease
Not applicable

Graham Little-Piccardi-Lassueur syndrome

ORPHA:505Disease

Granular corneal dystrophy type I

ORPHA:98962Disease
Autosomal dominant

Granular corneal dystrophy type II

ORPHA:98963Disease
Autosomal dominant

Granulomatosis with polyangiitis

ORPHA:900Disease
Not applicable

Granulomatous mastitis

ORPHA:64722Disease

Granulomatous slack skin

ORPHA:33111Disease
Not applicable

Gray platelet syndrome

ORPHA:721Disease
Autosomal dominant, Autosomal recessive

Grayson-Wilbrandt corneal dystrophy

ORPHA:293375Disease
Autosomal dominant

Greenberg dysplasia

ORPHA:1426Disease
Autosomal recessive

Griscelli syndrome

ORPHA:381Disease
Autosomal recessive

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-intellectual disability-hepatopathy syndrome

ORPHA:541423Disease
Autosomal recessive

Growth retardation-mild developmental delay-chronic hepatitis syndrome

ORPHA:391366Disease
Autosomal recessive

Guanidinoacetate methyltransferase deficiency

ORPHA:382Disease
Autosomal recessive

Gynandroblastoma

ORPHA:99914Disease

Gyrate atrophy of choroid and retina

ORPHA:414Disease
Autosomal recessive

HANAC syndrome

ORPHA:73229Disease
Autosomal dominant

HELLP syndrome

ORPHA:244242Disease
Multigenic/multifactorial

HJV or HAMP-related hemochromatosis

ORPHA:79230Disease
Autosomal recessive