lung disease, immunodeficiency, and chromosome breakage syndrome;
MONDO:0014984Mondo
Findings
No curated finding names lung disease, immunodeficiency, and chromosome breakage syndrome; yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
20 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.
- Bronchiolitis obliteransHPOHP:0011946
- 1 of 1 reported patient
- Cerebral calcificationHPOHP:0002514
- 2 of 2 reported patients
- Decreased total CD4+ T cell proportionHPOHP:0032218
- 3 of 3 reported patients
- Decreased total CD8+ T cell proportionHPOHP:0005415
- 3 of 3 reported patients
- Failure to thrive in infancyHPOHP:0001531
- 4 of 4 reported patients
- Hypoplasia of the thymusHPOHP:0000778
- 3 of 3 reported patients
- Increased circulating IgM concentrationHPOHP:0003496
- 3 of 3 reported patients
- Increased sensitivity to ionizing radiationHPOHP:0011133
- 1 of 1 reported patient
- Reduced delayed hypersensitivityHPOHP:0002972
- 3 of 3 reported patients
- Eczematoid dermatitisHPOHP:0000964
- 2 of 4 reported patients
- Wide anterior fontanelHPOHP:0000260
- 2 of 4 reported patients · Congenital onset
- Increased circulating IgE concentrationHPOHP:0003212
- 1 of 3 reported patients
Show the remaining 8
- Axial hypotoniaHPOHP:0008936
- 1 of 4 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 1 of 4 reported patients
- HypertelorismHPOHP:0000316
- 1 of 4 reported patients
- Midface retrusionHPOHP:0011800
- 1 of 4 reported patients
- Small for gestational ageHPOHP:0001518
- 1 of 4 reported patients · Congenital onset
- Decreased antigen-specific T cell proliferationHPOHP:0031402
- Feeding difficulties
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.
- NSMCE3HGNC:7677
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- Limited · ClinGen · Autosomal recessive · 2026
Where it sits
- A kind of