Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23312
Gene Symbol: DMXL2
DMXL2
CUI: C4539881
Disease: DEAFNESS, AUTOSOMAL DOMINANT 71
DEAFNESS, AUTOSOMAL DOMINANT 71 		0.300 GeneticVariation UNIPROT A dominant variant in DMXL2 is linked to nonsyndromic hearing loss. 27657680

2017