MYOF

myoferlin
OMIM: 604603, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red MYOF in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 5.3
Latest signed off version: v5.0 (1 May 2024)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • ?Angioedema, hereditary, 7, OMIM:619366