Hereditary agammaglobulinaemia with profoundly reduced or absent B cells (Q39690): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/393046642 / rank | |||
Normal rank | |||
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 |
||
| 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. |
