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Level 2: Viral research
Version 1.142
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review
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
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Sources
- Expert Review Green
- IUIS Classification February 2018
- IUIS Classification December 2019
- GRID V2.0
- Victorian Clinical Genetics Services
- ESID Registry 20171117
- IUIS Classification December 2019
- IUIS Classification February 2018
- Victorian Clinical Genetics Services
- ESID Registry 20171117
- GRID V2.0
Phenotypes
- Immunodeficiency, common variable with lack of anti-pneumococcal antibody
- Common variable immunodeficiency disorders (CVID)
- Predominantly Antibody Deficiencies
- Pneumonia, bacterial infections, warts, thrombocytopenia
- Pneumonia, bacterial infections, warts, thrombocytopenia. neutropenia
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Version 4.202
Latest signed off version: v4.0
(22 Mar 2023)
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review
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
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Sources
- IUIS Classification December 2019
- Expert Review Red
- IUIS Classification February 2018
- Victorian Clinical Genetics Services
- ESID Registry 20171117
- GRID V2.0
Phenotypes
- Common variable immunodeficiency disorders (CVID)
- Immunodeficiency, common variable with lack of anti-pneumococcal antibody
- Pneumonia, bacterial infections, warts, thrombocytopenia. neutropenia
- Predominantly Antibody Deficiencies
- Pneumonia, bacterial infections, warts, thrombocytopenia
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Version 1.184
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review
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BIALLELIC, autosomal or pseudoautosomal
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Sources
- Next Generation Children Project
- Expert Review Red
- Expert list
Phenotypes
- ?Immunodeficiency 16, 615593
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