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
- London North GLH
- GOSH PID v.8.0
- NHS GMS
- GRID V2.0
- Victorian Clinical Genetics Services
- North West GLH
- ESID Registry 20171117
- Combined B and T cell defect v1.12
- 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
- GOSH PID v.8.0
- Combined B and T cell defect v1.12
Phenotypes
- HLA class II deficiency
- Combined immunodeficiency (MHC class II deficiency, bare lymphocyte syndrome)
- Immunodeficiencies affecting cellular and humoral immunity
- Respiratory and gastrointestinal infections, liver/biliary tract disease
- Bare lymphocyte syndrome, type II, complementation group A
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Version 4.195
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
- Expert Review Green
- Other
- NHS GMS
- North West GLH
- London North GLH
- IUIS Classification February 2018
- Victorian Clinical Genetics Services
- ESID Registry 20171117
- GRID V2.0
- GOSH PID v.8.0
- Combined B and T cell defect v1.12
Phenotypes
- Bare lymphocyte syndrome, type II, complementation group A
- Combined immunodeficiency (MHC class II deficiency, bare lymphocyte syndrome)
- HLA class II deficiency
- Respiratory and gastrointestinal infections, liver/biliary tract disease
- Immunodeficiencies affecting cellular and humoral immunity
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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
- Bare lymphocyte syndrome, type II, complementation group A, 209920
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