International Classification of Diseases, 10th Edition, China

Last uploaded: November 11, 2019

Preferred Name	散光
ID	http://purl.bmicc.cn/ontology/ICD10CN/H52.2
cui	C0004106
free_Translation	http://purl.bioontology.org/ontology/ICD10/H52.2
has_exact_match	http://purl.bioontology.org/ontology/ICD10/H52.2
hasDbXref	UMLS_CUI:C0004106 SNOMEDCT_US_2016_03_01:193626006 ICD9CM:367.21 DOID:DOID_11782 CSP:1116-1831 DOID:DOID_13919 ICD9CM:367.20 EFO:0004222 HP:0000483 SNOMEDCT_US_2016_03_01:193627002 MESH:D001251 SNOMEDCT_US_2016_03_01:155134009 SNOMEDCT_US_2016_03_01:82649003 SNOMEDCT_US_2016_03_01:68905002 DOID:DOID_11781 ICD9CM:367.2 OMIM:603047 UMLS_CUI:C0152193
hasSTY	http://purl.bioontology.org/ontology/STY/T047
label	H52.2 散光
notation	H52.2
prefixIRI	ICD10CN:H52.2
prefLabel	散光
tui	T047
subClassOf	http://purl.bmicc.cn/ontology/ICD10CN/H52

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/ICD10/H52.2	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/OMIM/603047	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/ICD10CM/H52.20	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/D001251	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU011134	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/ICD10CM/H52.2	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0004106	MedlinePlus Health Topics	CUI