Human Disease Ontology / 人类疾病本体

Last uploaded: September 7, 2023

Preferred Name	cortical blindness
ID	http://purl.obolibrary.org/obo/DOID_11831
database_cross_reference	MESH:D019575 ICD10CM:H47.61 NCI:C118707 ICD9CM:377.75 UMLS_CUI:C0155320 SNOMEDCT_US_2022_09_01:68574006
has_obo_namespace	disease_ontology
id	DOID:11831
in_subset	http://purl.obolibrary.org/obo/doid#NCIthesaurus
label	cortical blindness
notation	DOID:11831
prefLabel	cortical blindness
subClassOf	http://purl.obolibrary.org/obo/DOID_5691

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/MTHU037241	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	LOOM
http://purl.obolibrary.org/obo/DOID_11831	BioAssay Ontology / 生物活性分析本体	LOOM
http://purl.obolibrary.org/obo/DOID_11831	BioAssay Ontology / 生物活性分析本体	SAME_URI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118707	National Cancer Institute Thesaurus / 美国国家癌症研究所词典	LOOM
http://purl.obolibrary.org/obo/MONDO_0001385	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.bioontology.org/ontology/ICD10CM/H47.61	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	LOOM