Autoimmune lymphoproliferative syndrome (Q84637): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
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 |
|---|---|---|---|
| default for all languages | ID_1072688797 |
||
| 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. |
Statements
CID11:ID_1072688797
0 references
dki-india-ID_1072688797
0 references
Concluído
0 references
13 August 2026
0 references
