EPX

eosinophil peroxidase
OMIM: 131399, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red EPX in Mendeliome


Version 1.2302

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