HMX1, H6 family homeobox 1, 3166

N. diseases: 23; N. variants: 1
Disease: Microphthalmos ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026010
Disease: Microphthalmos
Microphthalmos 		0.410 Biomarker disease CTD_human Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. 19379485 2009
CUI: C0026010
Disease: Microphthalmos
Microphthalmos 		0.410 PosttranslationalModification disease 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
CUI: C0026010
Disease: Microphthalmos
Microphthalmos 		0.410 Biomarker disease HPO