Human Phenotype Ontology / 人类表型本体

Last uploaded: September 7, 2023

Preferred Name	Choroideremia
ID	http://purl.obolibrary.org/obo/HP_0001139
database_cross_reference	UMLS:C0008525 MSH:D015794 SNOMEDCT_US:75241009
has_obo_namespace	human_phenotype
id	HP:0001139
label	Choroideremia
notation	HP:0001139
prefLabel	Choroideremia
treeView	http://purl.obolibrary.org/obo/HP_0000610
subClassOf	http://purl.obolibrary.org/obo/HP_0000610

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/303100	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	LOOM
http://purl.bioontology.org/ontology/ICD10CM/H31.21	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34469	National Cancer Institute Thesaurus / 美国国家癌症研究所词典	LOOM
http://purl.obolibrary.org/obo/MONDO_0010557	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0010557	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.bioontology.org/ontology/MESH/D015794	Medical Subject Headings / 医学主题词表	LOOM
http://www.orpha.net/ORDO/Orphanet_180	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
http://purl.obolibrary.org/obo/DOID_9821	BioAssay Ontology / 生物活性分析本体	LOOM
http://purl.obolibrary.org/obo/DOID_9821	Human Disease Ontology / 人类疾病本体	LOOM