Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3166
Gene Symbol: HMX1
HMX1
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		0.320 GeneticVariation BEFREE Identification of this causal mutation in the HMX1 gene indicates the role of this particular gene in the development of the external ear and provides a genetic marker for selection against microtia. 31691317

2020
Entrez Id: 3166
Gene Symbol: HMX1
HMX1
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		0.320 Biomarker BEFREE The coding regions of three genes, EVC known for cartilage development and NKX3-2, HMX1 involved in microtia, were selected for sequencing with 5 individuals from the pedigree. 24983964

2014
Entrez Id: 3166
Gene Symbol: HMX1
HMX1
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		0.320 Biomarker GENOMICS_ENGLAND Assignment of the murine Hmx1 homeobox gene to the proximal region of mouse chromosome 5. 9337406

1997