DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Cerebral Palsy ×

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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:	4842
Gene Symbol:	NOS1

NOS1

CUI:	C0007789
Disease:	Cerebral Palsy

Cerebral Palsy

0.010

GeneticVariation

BEFREE

The purpose of this study was to determine whether genetic variants of NOS1 contribute to CP susceptibility in a Han Chinese population.

2018