Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3166
Gene Symbol: HMX1
HMX1
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
0.410 Biomarker CTD_human Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. 19379485

2009

Entrez Id: 3166
Gene Symbol: HMX1
HMX1
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
0.410 PosttranslationalModification BEFREE Morpholino knockdown expression of the zebrafish nkx5-3 induced microphthalmia and disorganization of the developing retina, thus confirming that this gene represents an additional member implicated in axial patterning of the retina. 18423520

2008

Entrez Id: 3166
Gene Symbol: HMX1
HMX1
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
0.410 Biomarker HPO