Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 401
Gene Symbol: PHOX2A
PHOX2A
CUI: C0016059
Disease: Fibrosis
Fibrosis 		0.010 GeneticVariation LHGDN A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2). 14597037

2003