Preferred Name

Cleft Palate

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C87069

code

C87069

Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C158520

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C89506

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C186315

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C156952

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C158035

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C186341

Contributing_Source

CPTAC

NICHD

Cellosaurus

PCDC

DEFINITION

A congenital abnormality consisting of a fissure in the midline of the hard and/or soft palate; it is the result of the failure of the two sides of the palate to fuse during embryonic development.

FULL_SYN

Cleft Palate

label

Cleft Palate

Preferred_Name

Cleft Palate

prefixIRI

Thesaurus:C87069

prefLabel

Cleft Palate

Semantic_Type

Disease or Syndrome

UMLS_CUI

C0008925

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27651

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2849

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http://purl.bioontology.org/ontology/MESH/D002972 Medical Subject Headings / 医学主题词表 LOOM
http://purl.obolibrary.org/obo/MONDO_0016064 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0016064 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/DOID_674 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_674 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/HP_0000175 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/HP_0000175 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0008925 MedlinePlus Health Topics / MedlinePlus网站健康主题 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/LA42 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://www.orpha.net/ORDO/Orphanet_2014 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU000511 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU042142 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q35 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 LOOM
http://purl.bioontology.org/ontology/ICD10/Q35 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.bioontology.org/ontology/LNC/LA14412-3 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM