MPO:Ensemblv90

myeloperoxidase
OMIM: 606989, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber MPO in Mendeliome


Version 1.3802

1 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 1.45

Component of the following Super Panels:

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

    Amber MPO in Phagocyte Defects


    Level 2: Immunological disorders
    Version 2.0

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