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Preferred Name

唇裂和腭裂
ID

http://purl.bmicc.cn/ontology/ICD10CN/Q35-Q37.9
cui

C0158646
EXCLUDES1

罗宾氏徵候群(Robin'ssyndrome)(Q87.0)
free_Translation

http://purl.bioontology.org/ontology/ICD10/Q35-Q37.9
has_exact_match

http://purl.bioontology.org/ontology/ICD10/Q35-Q37.9
hasSTY

http://purl.bioontology.org/ontology/STY/T019
label

Q35-Q37 唇裂和腭裂
notation

Q35-Q37
prefixIRI

ICD10CN:Q35-Q37.9
prefLabel

唇裂和腭裂
tui

T019
subClassOf

http://purl.bmicc.cn/ontology/ICD10CN/Q00-Q99.9
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http://purl.bioontology.org/ontology/MEDLINEPLUS/C0158646 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/ICD10/Q35-Q37.9 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10CM/Q35-Q37 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/MTHU015010 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10/Q37 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU001582 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/LNC/LA14413-1 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/ICD10CM/Q37 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/MTHU017694 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10CM/Q37.9 International Classification of Diseases, Version 10 - Clinical Modification CUI