MPO

myeloperoxidase
OMIM: 606989, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber MPO in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Myeloperoxidase deficiency, MIM# 254600