immunodeficiency 53
MONDO:0054696Mondo
Findings
No curated finding names immunodeficiency 53 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
10 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Chronic coughHPOHP:0034315
- 3 of 3 reported patients
- Impaired phytohemagglutinin-induced T lymphocyte transformationHPOHP:0025834
- 3 of 3 reported patients
- Increased total neutrophil countHPOHP:0011897
- 3 of 3 reported patients
- Recurrent pneumoniaHPOHP:0006532
- 3 of 3 reported patients
- Recurrent otitis mediaHPOHP:0000403
- 2 of 3 reported patients
- AsthmaHPOHP:0002099
- 1 of 3 reported patients
- Failure to thriveHPOHP:0001508
- 1 of 3 reported patients
- Recurrent upper respiratory tract infectionsHPOHP:0002788
- 1 of 3 reported patients
- Recurrent urinary tract infectionsHPOHP:0000010
- 1 of 3 reported patients
- Skin rashHPOHP:0000988
- 1 of 3 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- RELBHGNC:9956
- Definitive · ClinGen · Autosomal recessive · 2026
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2018
Where it sits
- A kind of