Autoimmune Lymphoproliferative Syndrome
Disease ID: disease_node_12281
Connections displayed (default: 10).
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| Dbxref | GARD:8686, ICD10CM:D89.82, ICD9CM:279.41, MESH:D056735, MIM:601859, NCI:C37864, ORDO:3261, SNOMEDCT_US_2023_03_01:702444009, UMLS_CUI:C1328840 |
|---|---|
| Subclassof | DOID_2916 |
| Data Source | DOID, MESH |
| Synonyms | ALPS, Canale-Smith syndrome |
| Mesh Id | D056735 |
| Mesh Label | Autoimmune Lymphoproliferative Syndrome |
| Mesh Subclassof | D008232, D001327, D030342 |
| Doid Label | autoimmune lymphoproliferative syndrome |
| Doid Description | A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
| Disease Node Id | disease_node_12281 |
| Doid Id | DOID_6688 |
| Label | Autoimmune Lymphoproliferative Syndrome |
- Incoming r'ship
SUBCLASS_OFto/from Autoimmune Lymphoproliferative Syndrome Type 2B(ID:disease_node_13532) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Autoimmune Lymphoproliferative Syndrome Type 3(ID:disease_node_13530) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Immunoproliferative Disorders(ID:disease_node_4258) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Autoimmune Lymphoproliferative Syndrome Type 4(ID:disease_node_13531) (Disease)