SRP19

signal recognition particle 19
OMIM: 182175, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber SRP19 in Bone Marrow Failure


Level 2: Haematological disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Amber
Phenotypes
  • Neutropenia, MONDO:0001475, SRP19-related

Amber SRP19 in Phagocyte Defects


Level 2: Immunological disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Amber
Phenotypes
  • Neutropenia, MONDO:0001475, SRP19-related