CDH15

cadherin 15
OMIM: 114019, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CDH15 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Mental retardation, autosomal dominant 3, MIM#612580
Tags
  • disputed

Red CDH15 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
  • Mental retardation, autosomal dominant 3 MIM#612580
Tags
  • disputed