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Preferred Name

Meningioma
ID

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0025286
cui

C0025286
Inverse of RQ

http://purl.bioontology.org/ontology/MEDLINEPLUS/C0006118
notation

C0025286
prefLabel

Meningioma
tui

T191
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http://purl.obolibrary.org/obo/MPATH_251 中国人类表型本体 / Human Phenotype Ontology China LOOM
http://purl.obolibrary.org/obo/DOID_3565 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_3565 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU003590 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU003590 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/HP_0002858 Human Phenotype Ontology / 人类表型本体 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3230 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/MESH/D008579 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D008579 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/OMIM/601728 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/190040 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://www.orpha.net/ORDO/Orphanet_2495 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bioontology.org/ontology/ICD10CM/D32.9 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU036996 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.obolibrary.org/obo/MONDO_0016642 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0016642 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/NCIT_C3230 中国人类表型本体 / Human Phenotype Ontology China LOOM