loading...| Preferred Name |
autoimmune lymphoproliferative syndrome |
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| Synonyms |
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| Definitions |
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]. |
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| ID |
http://purl.obolibrary.org/obo/DOID_6688 |
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| comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
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| definition |
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. |
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| hasDbXref |
SNOMEDCT_US_2016_03_01:702444009 ICD9CM:279.41 NCI:C37864 ICD10CM:D47.9 ORDO:3261 OMIM:601859 ICD10CM:D89.82 UMLS_CUI:C1328840 CSP:1560-5548 MESH:D056735 |
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| hasExactSynonym |
Canale-Smith syndrome ALPS (autoimmune lymphoproliferative syndrome) |
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| hasOBONamespace |
disease_ontology |
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| id |
DOID:6688 |
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| imported from | ||
| inSubset | ||
| label |
autoimmune lymphoproliferative syndrome |
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| prefixIRI |
DOID:6688 |
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| prefLabel |
autoimmune lymphoproliferative syndrome |
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| subClassOf |
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