Hereditary agammaglobulinaemia with profoundly reduced or absent B cells (Q39690): Difference between revisions
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Revision as of 05:12, 13 August 2026
This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability to fight infection.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 4A01.00 |
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| English | Hereditary agammaglobulinaemia with profoundly reduced or absent B cells |
This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability to fight infection. |
Statements
CID11:4A01.00
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