EPHA10

EPH receptor A10
OMIM: 611123, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red EPHA10 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • postlingual non-syndromic genetic hearing loss, MONDO:0016298