immunodeficiency 77
MONDO:0030973Mondo
Findings
No curated finding names immunodeficiency 77 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
- Adult onset
HPO, annotations 2026-09-02
Features
8 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.
- Bilateral sensorineural hearing impairmentHPOHP:0008619
- 1 of 1 reported patient
- BronchiectasisHPOHP:0002110
- 4 of 4 reported patients
- CellulitisHPOHP:0100658
- 1 of 1 reported patient
- Cutaneous abscessHPOHP:0031292
- 1 of 1 reported patient
- GastroparesisHPOHP:0002578
- 1 of 1 reported patient
- Nontuberculous mycobacterial pulmonary infectionHPOHP:0032261
- 4 of 4 reported patients
- Recurrent tonsillitisHPOHP:0011110
- 1 of 1 reported patient
- Chronic pulmonary obstructionHPOHP:0006510
- 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.
- MPEG1HGNC:29619
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2021
Where it sits
- A kind of
Other names
1 name
Resolves to: immunodeficiency 77
- Also called
- IMD77