SRP19

signal recognition particle 19
OMIM: 182175, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber SRP19 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.93

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

Amber SRP19 in Mendeliome


Version 1.1891

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

Amber SRP19 in Phagocyte Defects


Level 2: Immunological disorders
Version 1.29

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Neutropenia, MONDO:0001475, SRP19-related