EPX

eosinophil peroxidase
OMIM: 131399, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red EPX in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • [Eosinophil peroxidase deficiency] MIM#261500