SRP68:Ensemblv115

signal recognition particle 68
OMIM: 604858, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber SRP68 in Phagocyte Defects


Level 2: Immunological disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • Neutropenia, severe congenital, 10, autosomal recessive, MIM# 620534