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The Human Phenotype Ontology is a standard vocabulary of clinical features (signs, symptoms, findings) with codes, used to describe patients in a way computers can compare.
The Human Phenotype Ontology is a formal ontology of human phenotypes developed within the Monarch Initiative and the OBO Foundry, with over 13,000 terms and annotations to hereditary diseases (Wikipedia). Terms such as weight loss or lymphadenopathy code clinical findings in records and registries; in oncology it is used less than NCIt, but it is the standard for phenotypes in rare disease and germline cancer predisposition.
Shares Mondo disease ontology, NCI Thesaurus (NCIt), Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares NCI Thesaurus (NCIt), Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares NCI Thesaurus (NCIt), Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Units of measurement ontology (UO), Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Units of measurement ontology (UO), Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Uberon anatomy ontology and the Cell Ontology, Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.
Shares Cancer AI vocabulary (CanSim terms map) and the tag cansim-terms.