Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3166
Gene Symbol: HMX1
HMX1
CUI: C2677500
Disease: Oculoauricular Syndrome
Oculoauricular Syndrome 		0.910 GeneticVariation BEFREE Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation. 29140751

2018