Combined Phenotype Ontology

Last uploaded: November 18, 2021
Preferred Name

Clinical modifier

Synonyms

Phenotypic modifier

Definitions

Note that some of the terms, such as Intellectual disability, have children terms such as Severe intellectual disability that represent precomposed combinations of modifiers and phenotypic abnormality terms. This done where the medical community commonly uses these terms with a fixed meaning (for instance, the Intellectual disability terms are used with specific IQ ranges). For computational reasoning, the semantics are intended to be the same as if there was a combination of the phenotype term and the clinical modifier term. This subontology is designed to provide terms to characterize and specify the phenotypic abnormalities defined in the Phenotypic abnormality subontology, with respect to severity, laterality, age of onset, and other aspects.

ID

http://purl.obolibrary.org/obo/HP_0012823

comment

Note that some of the terms, such as Intellectual disability, have children terms such as Severe intellectual disability that represent precomposed combinations of modifiers and phenotypic abnormality terms. This done where the medical community commonly uses these terms with a fixed meaning (for instance, the Intellectual disability terms are used with specific IQ ranges). For computational reasoning, the semantics are intended to be the same as if there was a combination of the phenotype term and the clinical modifier term.

creation date

2014-06-06T06:34:24Z

creator

https://orcid.org/0000-0002-0736-9199

database_cross_reference

UMLS:C4021064

definition

This subontology is designed to provide terms to characterize and specify the phenotypic abnormalities defined in the Phenotypic abnormality subontology, with respect to severity, laterality, age of onset, and other aspects.

has exact synonym

Phenotypic modifier

has_alternative_id

HP:0000004

id

HP:0012823

label

Clinical modifier

notation

HP:0012823

prefLabel

Clinical modifier

subClassOf

http://purl.obolibrary.org/obo/HP_0000001

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