KLHL10

kelch like family member 10
OMIM: 608778, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber KLHL10 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Spermatogenic failure 11, MIM# 615081