Jump to:
Spinner 000000 16px loading...
Preferred Name

CR(E)ST syndrome
Synonyms

Combination of calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia
ID

http://purl.bioontology.org/ontology/ICD10CM/M34.1
altLabel

Combination of calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia
cui

C2895195

C0206138
Inverse of SIB

http://purl.bioontology.org/ontology/ICD10CM/M34.8

http://purl.bioontology.org/ontology/ICD10CM/M34.2

http://purl.bioontology.org/ontology/ICD10CM/M34.0

http://purl.bioontology.org/ontology/ICD10CM/M34.9
notation

M34.1
Order number

18204
prefLabel

CR(E)ST syndrome
tui

T047
subClassOf

http://purl.bioontology.org/ontology/ICD10CM/M34
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70646 National Cancer Institute Thesaurus LOOM
http://purl.bmicc.cn/ontology/ICD10CN/M34.1 International Classification of Diseases, 10th Edition, China CUI
http://purl.obolibrary.org/obo/DOID_0060218 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/ICD10/M34.1 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10/M34.1 International Classification of Diseases, Version 10 LOOM
http://purl.bioontology.org/ontology/MESH/D017675 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D017675 Medical Subject Headings LOOM
http://purl.bioontology.org/ontology/OMIM/181750 Online Mendelian Inheritance in Man CUI