Kidney Tissue Atlas Ontology

Last uploaded: March 16, 2024
Preferred Name

CREST syndrome

Synonyms

limited cutaneous Systemic Scleroderma

limited cutaneous Systemic sclerosis

calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome

lcSSc

calcinosis Raynaud phenomenon sclerodactyly telangiectasia

calcinosis - Raynaud phenomenon - esophageal involvement - sclerodactyly - telangiectasia

calcinosis, Raynaud's phenomenon, esophageal dismobility, sclerodactyly, telangiectasia syndrome

phenomenon-sclerodactyly-telangiectasia, calcinosis-Raynaud

syndrome, CREST

calcinosis-Raynaud phenomenon-sclerodactyly-telangiectasia

CRST syndrome

CRST syndromes

Definitions

CREST syndrome is a subtype of limited cutaneous systemic sclerosis (lcSSc) whose name is an acronym for the cardinal clinical features of the syndrome: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly and telangiectasia.

ID

http://purl.obolibrary.org/obo/MONDO_0019563

closeMatch

http://identifiers.org/snomedct/201442004

http://identifiers.org/snomedct/62382002

http://linkedlifedata.com/resource/umls/id/C1527226

http://identifiers.org/snomedct/156453002

database_cross_reference

Orphanet:90290

COHD:4135937

GARD:0012430

MedDRA:10011380

ICD10:M34.1

MESH:D017675

DOID:0060218

UMLS:C0206138

SCTID:31848007

NCIT:C70646

exactMatch

http://identifiers.org/meddra/10011380

http://purl.obolibrary.org/obo/NCIT_C70646

http://identifiers.org/snomedct/31848007

http://purl.obolibrary.org/obo/DOID_0060218

http://linkedlifedata.com/resource/umls/id/C0206138

http://www.orpha.net/ORDO/Orphanet_90290

http://identifiers.org/mesh/D017675

has broad synonym

lcSSc

has exact synonym

limited cutaneous Systemic Scleroderma

limited cutaneous Systemic sclerosis

calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome

has narrow synonym

CRST syndrome

CRST syndromes

has related synonym

calcinosis Raynaud phenomenon sclerodactyly telangiectasia

calcinosis - Raynaud phenomenon - esophageal involvement - sclerodactyly - telangiectasia

calcinosis, Raynaud's phenomenon, esophageal dismobility, sclerodactyly, telangiectasia syndrome

phenomenon-sclerodactyly-telangiectasia, calcinosis-Raynaud

syndrome, CREST

calcinosis-Raynaud phenomenon-sclerodactyly-telangiectasia

id

MONDO:0019563

imported from

http://purl.obolibrary.org/obo/mondo.owl

in_subset

http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_clinical_subtype

label

CREST syndrome

notation

MONDO:0019563

prefLabel

CREST syndrome

textual definition

CREST syndrome is a subtype of limited cutaneous systemic sclerosis (lcSSc) whose name is an acronym for the cardinal clinical features of the syndrome: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly and telangiectasia.

subClassOf

http://purl.obolibrary.org/obo/MONDO_0006832

http://purl.obolibrary.org/obo/MONDO_0016358

http://purl.obolibrary.org/obo/MONDO_0016177

http://purl.obolibrary.org/obo/MONDO_0000774

http://purl.obolibrary.org/obo/MONDO_0002254

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Create mapping

Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0019563 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019563 DOVES SAME_URI
http://purl.obolibrary.org/obo/DOID_0060218 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0019563 MONDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C14.907.617.812.500 RH-MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0206138 OCHV LOOM
http://www.owl-ontologies.com/unnamed.owl#RID14086 DERMLEX LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D017675 RH-MESH LOOM
http://www.limics.fr/ontologies/ontolurgences#SyndromeCREST ONTOLURGENCES LOOM
http://purl.bioontology.org/ontology/RCTV2/N001100 RCTV2 LOOM
http://purl.obolibrary.org/obo/NCIT_C70646 BERO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.174.130.204 RH-MESH LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70646 NCIT LOOM
http://purl.bioontology.org/ontology/ICD10/M34.1 ICD10 LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#20818 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C14.907.823.225 RH-MESH LOOM
http://purl.obolibrary.org/obo/DOID_0060218 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0060218 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0060218 FNS-H LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038508 PMAPP-PMO LOOM
http://purl.bioontology.org/ontology/ICPC2P/A99013 ICPC2P LOOM
http://purl.obolibrary.org/obo/MONDO_0019563 DOVES LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/31848007 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/SNMI/D1-10240 SNMI LOOM
http://purl.jp/bio/4/id/200906009479487875 IOBC LOOM
http://purl.bioontology.org/ontology/MESH/D017675 MESH LOOM
http://www.orpha.net/ORDO/Orphanet_90290 ORDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C17.300.799.801.500 RH-MESH LOOM
http://purl.bioontology.org/ontology/MEDDRA/10011380 MEDDRA LOOM
http://purl.obolibrary.org/obo/OMIT_0017982 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C06.405.117.119.500.204 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C17.800.784.801.500 RH-MESH LOOM
http://purl.bioontology.org/ontology/ICD10CM/M34.1 ICD10CM LOOM
http://www.limics.org/hrdo/rdfns#pat_id_12001 HRDO LOOM
http://www.gamuts.net/entity#CREST_syndrome GAMUTS LOOM
http://purl.obolibrary.org/obo/DERMO_0001906 DERMO LOOM