International Classification of Diseases Ontology

Last uploaded: February 24, 2022
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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
imported from

http://purl.obolibrary.org/obo/hp.owl
label

Myelopathy
notation

HP:0002196
prefLabel

Myelopathy
subClassOf

http://purl.obolibrary.org/obo/HP_0002011
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http://purl.obolibrary.org/obo/HP_0002196 Human Phenotype Ontology LOOM
http://purl.obolibrary.org/obo/HP_0002196 Human Phenotype 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