Level 2: Viral research
Version 1.142
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review
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BOTH monoallelic and biallelic, autosomal or pseudoautosomal
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Sources
- IUIS Classification February 2018
- 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
Phenotypes
- Angioedema, hereditary, types I and II 106100
- Complement component 4, partial deficiency of 120790
- Complement Deficiencies
- Hereditary Angioedema (C1inh)
- Hereditary angioedema
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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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BOTH monoallelic and 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
Phenotypes
- Angioedema, hereditary, types I and II 106100
- Hereditary Angioedema (C1inh)
- Complement component 4, partial deficiency of 120790
- Hereditary angioedema
- Complement Deficiencies
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Version 1.184
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review
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BOTH monoallelic and biallelic, autosomal or pseudoautosomal
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Sources
- Next Generation Children Project
- Expert Review Green
- Expert list
Phenotypes
- Complement component 4, partial deficiency of, 120790
- Angioedema, hereditary, types I and II, 106100
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Version 1.1
Latest signed off version: v1.0
(14 Sep 2023)
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review
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BOTH monoallelic and biallelic, autosomal or pseudoautosomal
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Sources
- NHS GMS
- Expert Review Green
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