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Level 2: Viral research
Version 1.142
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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
- Lymphoproliferative syndrome 2
- Combined immunodeficiency
- Diseases of Immune Dysregulation
- Features triggered by EBV infection, HLH, aplastic anemia, low iNKT cells, lymphoma
- Combined immunodeficiency with EBV-associated lymphoproliferation
- CD27 deficiency
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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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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
- Lymphoproliferative syndrome 2
- Combined immunodeficiency with EBV-associated lymphoproliferation
- Combined immunodeficiency
- CD27 deficiency
- Features triggered by EBV infection, HLH, aplastic anemia, low iNKT cells, lymphoma
- Diseases of Immune Dysregulation
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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 Green
- Expert list
Phenotypes
- Lymphoproliferative syndrome 2, 615122
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