DisGeNET - a database of gene-disease associations

Gene: ARMC4 ×

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:	55130
Gene Symbol:	ARMC4

ARMC4

CUI:	C1853444
Disease:	Heterotaxy, Visceral, 3, Autosomal

Heterotaxy, Visceral, 3, Autosomal

0.200

Biomarker

MGD

ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry.

2013