immunodeficiency, developmental delay, and hypohomocysteinemia
MONDO:0060591Mondo
Findings
No curated finding names immunodeficiency, developmental delay, and hypohomocysteinemia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
25 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.
- Decreased serum creatinineHPOHP:0012101
- 4 of 4 reported patients
- Mild global developmental delayHPOHP:0011342
- 4 of 4 reported patients
- Recurrent lower respiratory tract infectionsHPOHP:0002783
- 4 of 4 reported patients
- Failure to thriveHPOHP:0001508
- 3 of 4 reported patients
- HypohomocysteinemiaHPOHP:0020222
- 3 of 4 reported patients
- Recurrent skin infectionsHPOHP:0001581
- 3 of 4 reported patients
- Delayed skeletal maturationHPOHP:0002750
- 2 of 3 reported patients
- HeadacheHPOHP:0002315
- 2 of 3 reported patients
- Short statureHPOHP:0004322
- 2 of 3 reported patients
- Atrial septal defectHPOHP:0001631
- 2 of 4 reported patients
- HypocystinemiaHPOHP:0500152
- 2 of 4 reported patients
- Muscle weaknessHPOHP:0001324
- 2 of 4 reported patients
Show the remaining 13
- Bicuspid aortic valveHPOHP:0001647
- 1 of 4 reported patients
- Decreased circulating IgA concentrationHPOHP:0002720
- 1 of 4 reported patients
- Decreased circulating immunoglobulin concentrationHPOHP:0004313
- 1 of 4 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 1 of 4 reported patients
- Easy fatigabilityHPOHP:0003388
- 1 of 4 reported patients
- Feeding difficultiesHPOHP:0011968
- 1 of 4 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.
- NFE2L2HGNC:7782
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- Strong · G2P · Autosomal dominant · 2021
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Limited · ClinGen · Autosomal dominant · 2025
- Limited · Illumina · Autosomal dominant · 2021
Where it sits
- A kind of