Autoimmune lymphoproliferative syndrome (Q84637): Difference between revisions
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Síndrome linfoproliferativa autoimune (ALPS) é um transtorno genético associado a apoptose anormal de linfócitos, linfoproliferação e autoimunidade. Manifestações comuns são graves linfadenopatia e esplenomegalia, anemia hemolítica, neutropenia autoimune e púpura trombocitopênica imune. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Autoimmune lymphoproliferative syndrome (ALPS) is a genetic disorder associated with abnormal lymphocyte apoptosis, lymphoproliferation, and autoimmunity. Common features are severe lymphadenopathy and splenomegaly, haemolytic anaemia, autoimmune neutropaenia, and immune thrombocytopenia purpura. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1072688797 / rank | |||||||||||||||
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CID11:ID_1072688797 | |||||||||||||||
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dki-india-ID_1072688797 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 09:59, 15 August 2026
Autoimmune lymphoproliferative syndrome (ALPS) is a genetic disorder associated with abnormal lymphocyte apoptosis, lymphoproliferation, and autoimmunity. Common features are severe lymphadenopathy and splenomegaly, haemolytic anaemia, autoimmune neutropaenia, and immune thrombocytopenia purpura.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1072688797 |
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| English | Autoimmune lymphoproliferative syndrome |
Autoimmune lymphoproliferative syndrome (ALPS) is a genetic disorder associated with abnormal lymphocyte apoptosis, lymphoproliferation, and autoimmunity. Common features are severe lymphadenopathy and splenomegaly, haemolytic anaemia, autoimmune neutropaenia, and immune thrombocytopenia purpura. |
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CID11:ID_1072688797
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dki-india-ID_1072688797
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Concluído
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13 August 2026
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