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Preferred Name

未特指的强迫性障碍
ID

http://purl.bmicc.cn/ontology/ICD10CN/F42.9
cui

C0028768
free_Translation

http://purl.bioontology.org/ontology/ICD10/F42.9
has_exact_match

http://purl.bioontology.org/ontology/ICD10/F42.9
hasSTY

http://purl.bioontology.org/ontology/STY/T048
label

F42.9 未特指的强迫性障碍
notation

F42.9
prefixIRI

ICD10CN:F42.9
prefLabel

未特指的强迫性障碍
tui

T048
subClassOf

http://purl.bmicc.cn/ontology/ICD10CN/F42
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http://purl.bioontology.org/ontology/ICD10CM/F42 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/164230 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/LNC/LA10581-9 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/OMIM/MTHU007292 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10CM/F42.8 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0028768 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/ICD10/F42 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/MESH/D009771 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/ICD10/F42.9 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU000246 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10CM/F42.9 International Classification of Diseases, Version 10 - Clinical Modification CUI