HOXD10

homeobox D10
OMIM: 142984, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red HOXD10 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Charcot-Marie-Tooth disease, foot deformity of
  • Vertical talus, congenital (MIM#192950)

Red HOXD10 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Vertical talus, congenital, MIM#192950