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
- Combined immunodeficiency
- Immunodeficiency 8
- hypogammaglobulinaemia, combined immunodeficiency
- Coronin-1A deficiency
- Atypical Severe Combined Immunodeficiency (Atypical SCID)
- Detectable thymus, EBV
- Immunodeficiencies affecting cellular and humoral immunity
- Omenn syndrome
- Severe combined immunodeficiency (SCID)
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Version 1.6
Latest signed off version: v1.3
(15 Oct 2020)
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review
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BIALLELIC, autosomal or pseudoautosomal
|
Sources
|
Version 4.196
Latest signed off version: v4.0
(22 Mar 2023)
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review
|
BIALLELIC, autosomal or pseudoautosomal
|
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
- Immunodeficiency 8
- Combined immunodeficiency
- hypogammaglobulinaemia, combined immunodeficiency
- Coronin-1A deficiency
- Atypical Severe Combined Immunodeficiency (Atypical SCID)
- Severe combined immunodeficiency (SCID)
- Omenn syndrome
- Detectable thymus, EBV
- Immunodeficiencies affecting cellular and humoral immunity
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Version 1.182
|
review
|
BIALLELIC, autosomal or pseudoautosomal
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Sources
- Next Generation Children Project
- Expert Review Green
- Expert list
Phenotypes
- Immunodeficiency 8, 615401
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