MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Gray platelet syndrome

ORPHA:721Kr.
Autosomal dominant, Autosomal recessive

Grayson-Wilbrandt corneal dystrophy

ORPHA:293375Kr.
Autosomal dominant

Greenberg dysplasia

ORPHA:1426Kr.
Autosomal recessive

Greig cephalopolysyndactyly syndrome

ORPHA:380Malf.
Autosomal dominant

Greig cephalopolysyndactyly-contiguous gene syndrome

ORPHA:658805Malf.

Griscelli syndrome

ORPHA:381Kr.
Autosomal recessive

Griscelli syndrome type 1

ORPHA:79476Kl. subt.
Autosomal recessive

Griscelli syndrome type 2

ORPHA:79477Kl. subt.
Autosomal recessive

Griscelli syndrome type 3

ORPHA:79478Kl. subt.
Autosomal recessive

Grisel syndrome

ORPHA:662255Clinical syndrome
Not applicable

Growing teratoma syndrome

ORPHA:314613spez. Sit.
Not applicable

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-hydrocephaly-lung hypoplasia syndrome

ORPHA:3035Malf.

Growth delay-intellectual disability-hepatopathy syndrome

ORPHA:541423Kr.
Autosomal recessive

Growth retardation-mild developmental delay-chronic hepatitis syndrome

ORPHA:391366Kr.
Autosomal recessive

Grubben-de Cock-Borghgraef syndrome

ORPHA:2101Malf.

Guanidinoacetate methyltransferase deficiency

ORPHA:382Kr.
Autosomal recessive

Guillain-Barré syndrome

ORPHA:2103Kl. gruppe
Multigenic/multifactorial

Guttmacher syndrome

ORPHA:2957Malf.
Autosomal dominant

Gynandroblastoma

ORPHA:99914Kr.

Gyrate atrophy of choroid and retina

ORPHA:414Kr.
Autosomal recessive

Gómez-López-Hernández syndrome

ORPHA:1532Malf.
Not applicable