Immunodeficiency with CD46 deficiency (Q51693): Difference between revisions
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A deficiência de CD46 é um fator predisponente para inúmeras doenças decorrentes do “auto-ataque” mediado pelo complemento. Mutações no regulador do complemento humano, uma proteína cofator de membrana de (CD46), predispõem ao desenvolvimento da síndrome hemolítica urêmica familiar. | |||
| description / en | description / en | ||
Deficiency of CD46 is a predisposing factor for numerous disease conditions arising from complement-mediated ‘self-attack’. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial haemolytic uremic syndrome. | |||
Revision as of 22:54, 13 August 2026
Deficiency of CD46 is a predisposing factor for numerous disease conditions arising from complement-mediated ‘self-attack’. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial haemolytic uremic syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2034677150 |
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| English | Immunodeficiency with CD46 deficiency |
Deficiency of CD46 is a predisposing factor for numerous disease conditions arising from complement-mediated ‘self-attack’. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial haemolytic uremic syndrome. |
