MPO

myeloperoxidase
OMIM: 606989, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber MPO in Mendeliome


Version 1.2789

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

Amber MPO in Phagocyte Defects


Level 2: Immunological disorders
Version 1.35

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Other
    Phenotypes
    • myeloperoxidase deficiency MONDO:0009694