Level 2: Viral research
Version 1.141
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review
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BIALLELIC, autosomal or pseudoautosomal
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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
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Version 4.196
Latest signed off version: v4.0
(22 Mar 2023)
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review
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BIALLELIC, autosomal or pseudoautosomal
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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
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Version 1.182
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review
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BIALLELIC, autosomal or pseudoautosomal
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Sources
- Next Generation Children Project
- Expert Review Green
- Expert list
Phenotypes
- Immunodeficiency, common variable, 3, 613493
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