Human Phenotype Ontology

Last uploaded: February 24, 2022

Preferred Name	Myelopathy
ID	http://purl.obolibrary.org/obo/HP_0002196
database_cross_reference	UMLS:C0037928 MSH:D013118 SNOMEDCT_US:48522003
has_obo_namespace	human_phenotype
id	HP:0002196
label	Myelopathy
notation	HP:0002196
prefLabel	Myelopathy
treeView	http://purl.obolibrary.org/obo/HP_0002143
subClassOf	http://purl.obolibrary.org/obo/HP_0002143

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/HP_0002196	International Classification of Diseases Ontology	LOOM
http://purl.obolibrary.org/obo/HP_0002196	International Classification of Diseases Ontology	SAME_URI
http://purl.bioontology.org/ontology/OMIM/MTHU005441	Online Mendelian Inheritance in Man	LOOM
http://purl.bmicc.cn/ontology/ICD11CN/8B42	International Classification of Diseases, 11th Edition, China	LOOM