Hereditary agammaglobulinaemia with profoundly reduced or absent B cells (Q39690): Difference between revisions
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| description / pt-br | description / pt-br | ||
Refere-se a um tipo hereditário de imunodeficiência primária caracterizada por uma redução em todos os tipos de gamaglobulinas e um raro transtorno genético ligado ao X que afeta a capacidade do corpo de combater infecções. | |||
| description / en | description / en | ||
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. | |||
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. |
