Human Disease Ontology

Last uploaded: June 28, 2024
Preferred Name

autoimmune lymphoproliferative syndrome

Synonyms

Canale-Smith syndrome

ALPS

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].

ID

http://purl.obolibrary.org/obo/DOID_6688

comment

Xref MGI. OMIM mapping confirmed by DO. [SN].

database_cross_reference

SNOMEDCT_US_2023_03_01:702444009

ICD10CM:D89.82

UMLS_CUI:C1328840

ICD9CM:279.41

MESH:D056735

GARD:8686

MIM:601859

NCI:C37864

ORDO:3261

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.

has exact match

MESH:D056735

has exact synonym

Canale-Smith syndrome

ALPS

has_obo_namespace

disease_ontology

id

DOID:6688

in_subset

http://purl.obolibrary.org/obo/doid#NCIthesaurus

http://purl.obolibrary.org/obo/doid#DO_rare_slim

label

autoimmune lymphoproliferative syndrome

notation

DOID:6688

prefLabel

autoimmune lymphoproliferative syndrome

subClassOf

http://purl.obolibrary.org/obo/DOID_2916

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_6688 DTO SAME_URI
http://purl.obolibrary.org/obo/DOID_6688 BAO SAME_URI
http://purl.obolibrary.org/obo/DOID_6688 HHEAR SAME_URI
http://purl.obolibrary.org/obo/DOID_6688 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_6688 MIDO SAME_URI
http://purl.obolibrary.org/obo/DOID_6688 FNS-H SAME_URI
http://purl.obolibrary.org/obo/MONDO_0017979 MONDO LOOM
http://nanbyodata.jp/ontology/NANDO_1200352 NANDO LOOM
http://nanbyodata.jp/ontology/NANDO_2200726 NANDO LOOM
http://purl.obolibrary.org/obo/MONDO_0017979 EFO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C15.604.515.138 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00037428 PMAPP-PMO LOOM
http://purl.obolibrary.org/obo/NCIT_C37864 BERO LOOM
http://purl.bioontology.org/ontology/OMIM/601859 OMIM LOOM
http://purl.obolibrary.org/obo/MONDO_0017979 DOVES LOOM
http://purl.jp/bio/4/id/201006089431511795 IOBC LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.089 RH-MESH LOOM
http://purl.bioontology.org/ontology/PDQ/CDR0000739826 PDQ LOOM
http://purl.bioontology.org/ontology/ICD9CM/279.41 ICD9CM LOOM
http://purl.bioontology.org/ontology/ICD9CM/279.41 NLMVS LOOM
http://purl.obolibrary.org/obo/OMIT_0026704 OMIT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C37864 NCIT LOOM
http://www.orpha.net/ORDO/Orphanet_3261 ORDO LOOM
http://purl.bioontology.org/ontology/MESH/D056735 MESH LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/702444009 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/MEDDRA/10069521 MEDDRA LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C20.111.288 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C20.683.515.124 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D056735 RH-MESH LOOM
http://www.limics.org/hrdo/rdfns#pat_id_3468 HRDO LOOM
http://purl.obolibrary.org/obo/DOID_6688 DTO LOOM
http://purl.obolibrary.org/obo/DOID_6688 BAO LOOM
http://purl.obolibrary.org/obo/DOID_6688 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_6688 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_6688 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_6688 FNS-H LOOM
http://www.gamuts.net/entity#Canale_Smith_syndrome GAMUTS REST