Human Disease Ontology / 人类疾病本体

Last uploaded: September 7, 2023

Preferred Name	Phenotypic abnormality
ID	http://purl.obolibrary.org/obo/HP_0000118
id	HP:0000118
label	Phenotypic abnormality
notation	HP:0000118
prefixIRI	HP:0000118
prefLabel	Phenotypic abnormality
subClassOf	http://purl.obolibrary.org/obo/UPHENO_0001001

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/HP_0000118	中国人类表型本体 / Human Phenotype Ontology China	LOOM
http://purl.obolibrary.org/obo/HP_0000118	中国人类表型本体 / Human Phenotype Ontology China	SAME_URI
http://purl.obolibrary.org/obo/HP_0000118	Coronavirus Infectious Disease Ontology / 冠状病毒感染性疾病本体	LOOM
http://purl.obolibrary.org/obo/HP_0000118	Coronavirus Infectious Disease Ontology / 冠状病毒感染性疾病本体	SAME_URI
http://purl.obolibrary.org/obo/HP_0000118	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.obolibrary.org/obo/HP_0000118	Experimental Factor Ontology / 实验性因素本体	SAME_URI
http://purl.obolibrary.org/obo/HP_0000118	Human Phenotype Ontology / 人类表型本体	LOOM
http://purl.obolibrary.org/obo/HP_0000118	Human Phenotype Ontology / 人类表型本体	SAME_URI
http://purl.obolibrary.org/obo/HP_0000118	GenEpiO / 基因组流行病学本体	LOOM
http://purl.obolibrary.org/obo/HP_0000118	GenEpiO / 基因组流行病学本体	SAME_URI