|
Level 2: Viral research
Version 1.146
|
review
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
- IUIS Classification February 2018
- A- or hypo-gammaglobulinaemia v1.25
- London North GLH
- GOSH PID v.8.0
- 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
- GOSH PID v.8.0
- A- or hypo-gammaglobulinaemia v1.25
Phenotypes
- Hyper IgM syndrome with lymphoid hyperplasia
- Immunodeficiency with hyper IgM, type 5, 608106
- Enlarged lymph nodes and germinal centers
- Predominantly Antibody Deficiencies
- CSR defects and Hyper IgM (HIGM) syndromes
- Immunodeficiency with hyper IgM, type 5
|
|
Level 2: Immunology
Version 8.78
Latest signed off version: v8.0
(30 Apr 2025)
|
review
|
BIALLELIC, autosomal or pseudoautosomal
|
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
- GOSH PID v.8.0
- A- or hypo-gammaglobulinaemia v1.25
Phenotypes
- Immunodeficiency with hyper IgM, type 5
- Hyper IgM syndrome with lymphoid hyperplasia
- CSR defects and Hyper IgM (HIGM) syndromes
- Immunodeficiency with hyper IgM, type 5, 608106
- Enlarged lymph nodes and germinal centers
- Predominantly Antibody Deficiencies
|