DisGeNET - a database of gene-disease associations

Source: MGD

Disease: Tetralogy of Fallot ×

Gene: DNAH5 ×

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:	1767
Gene Symbol:	DNAH5

DNAH5

CUI:	C0039685
Disease:	Tetralogy of Fallot

Tetralogy of Fallot

0.200

Biomarker

MGD

Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia.

2007