HMX1, H6 family homeobox 1, 3166

N. diseases: 23; N. variants: 1
Disease: Retinal Dystrophies ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		0.010 GeneticVariation group BEFREE Retinal dystrophy in the oculo-auricular syndrome due to HMX1 mutation. 21417677 2011