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
notation

M34.1
Order number

18848
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 / 美国国家癌症研究所词典 LOOM
http://www.orpha.net/ORDO/Orphanet_90290 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bmicc.cn/ontology/ICD10CN/M34.1 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.obolibrary.org/obo/DOID_0060218 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/ICD10/M34.1 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/ICD10/M34.1 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.obolibrary.org/obo/MONDO_0019563 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.bioontology.org/ontology/MESH/D017675 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D017675 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/OMIM/181750 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI