|
Level 2: Viral research
Version 1.147
|
review
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
- IUIS Classification February 2018
- A- or hypo-gammaglobulinaemia v1.25
- London North GLH
- NHS GMS
- GRID V2.0
- Victorian Clinical Genetics Services
- North West GLH
- ESID Registry 20171117
- Expert Review Green
- NHS GMS
- North West GLH
- London North GLH
- IUIS Classification February 2018
- Victorian Clinical Genetics Services
- Expert Review Green
- ESID Registry 20171117
- GRID V2.0
- A- or hypo-gammaglobulinaemia v1.25
Phenotypes
- Immunodeficiency, common variable, 3
- Isolated IgG subclass deficiency
- Recurrent infections, may have glomerulonephritis
- Immunodeficiency, common variable, 3 613493
- Common variable immunodeficiency disorders (CVID)
- Predominantly Antibody Deficiencies
- hypogammaglobulinemia
|
|
Level 2: Immunology
Version 8.85
Latest signed off version: v8.0
(30 Apr 2025)
|
review
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
- NHS GMS
- North West GLH
- London North GLH
- IUIS Classification February 2018
- Victorian Clinical Genetics Services
- Expert Review Green
- ESID Registry 20171117
- GRID V2.0
- A- or hypo-gammaglobulinaemia v1.25
Phenotypes
- Immunodeficiency, common variable, 3 613493
- hypogammaglobulinemia
- Immunodeficiency, common variable, 3
- Common variable immunodeficiency disorders (CVID)
- Isolated IgG subclass deficiency
- Recurrent infections, may have glomerulonephritis
- Predominantly Antibody Deficiencies
|