MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Gonadoblastoma

ORPHA:206484Kr.

Gonococcal conjunctivitis

ORPHA:1482Kr.

Graft versus host disease

ORPHA:39812Kr.
Not applicable

Graham Little-Piccardi-Lassueur syndrome

ORPHA:505Kr.

Granular corneal dystrophy type I

ORPHA:98962Kr.
Autosomal dominant

Granular corneal dystrophy type II

ORPHA:98963Kr.
Autosomal dominant

Granulomatosis with polyangiitis

ORPHA:900Kr.
Not applicable

Granulomatous mastitis

ORPHA:64722Kr.

Granulomatous slack skin

ORPHA:33111Kr.
Not applicable

Gray platelet syndrome

ORPHA:721Kr.
Autosomal dominant, Autosomal recessive

Grayson-Wilbrandt corneal dystrophy

ORPHA:293375Kr.
Autosomal dominant

Greenberg dysplasia

ORPHA:1426Kr.
Autosomal recessive

Griscelli syndrome

ORPHA:381Kr.
Autosomal recessive

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

ORPHA:391348Kr.
Autosomal recessive

Growth delay due to insulin-like growth factor I resistance

ORPHA:73273Kr.
Autosomal dominant, Autosomal recessive

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

ORPHA:73272Kr.
Autosomal recessive

Growth delay-intellectual disability-hepatopathy syndrome

ORPHA:541423Kr.
Autosomal recessive

Growth retardation-mild developmental delay-chronic hepatitis syndrome

ORPHA:391366Kr.
Autosomal recessive

Guanidinoacetate methyltransferase deficiency

ORPHA:382Kr.
Autosomal recessive

Gynandroblastoma

ORPHA:99914Kr.

Gyrate atrophy of choroid and retina

ORPHA:414Kr.
Autosomal recessive

HANAC syndrome

ORPHA:73229Kr.
Autosomal dominant

HELLP syndrome

ORPHA:244242Kr.
Multigenic/multifactorial

HJV or HAMP-related hemochromatosis

ORPHA:79230Kr.
Autosomal recessive