DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Chronic granulomatous disease ×

Gene: CYBA ×

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:	1535
Gene Symbol:	CYBA

CYBA

CUI:	C0018203
Disease:	Chronic granulomatous disease

Chronic granulomatous disease

0.500

GeneticVariation

LHGDN

Here, we report the case of an autosomal recessive CGD patient with a defect in the p22 phox subunit.

2002