Human Phenotype Ontology

Last uploaded: February 24, 2022
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Preferred Name

Hypertensive retinopathy
ID

http://purl.obolibrary.org/obo/HP_0001095
database_cross_reference

SNOMEDCT_US:6962006

UMLS:C0152132

MSH:D058437
has_obo_namespace

human_phenotype
id

HP:0001095
in_subset

http://purl.obolibrary.org/obo/hp.obo#secondary_consequence
label

Hypertensive retinopathy
notation

HP:0001095
prefLabel

Hypertensive retinopathy
treeView

http://purl.obolibrary.org/obo/HP_0008046
subClassOf

http://purl.obolibrary.org/obo/HP_0008046
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http://purl.obolibrary.org/obo/DOID_11561 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/MESH/D058437 Medical Subject Headings LOOM
http://purl.bmicc.cn/ontology/ICD11CN/9B71.1 International Classification of Diseases, 11th Edition, China LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3514 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/ICD10CM/H35.03 International Classification of Diseases, Version 10 - Clinical Modification LOOM