DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Cerebral Palsy ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	2571
Gene Symbol:	GAD1

GAD1

CUI:	C0007789
Disease:	Cerebral Palsy

Cerebral Palsy

0.110

GeneticVariation

BEFREE

A novel amino acid mis-sense mutation in GAD67 was detected, which segregated with CP in affected individuals.

2004

Entrez Id:	2571
Gene Symbol:	GAD1

GAD1

CUI:	C0007789
Disease:	Cerebral Palsy

Cerebral Palsy

0.110

Biomarker

HPO