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Clinical modifier (HP:0012823)
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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.
Frequency +   
Mode of inheritance +   
Phenotypic abnormality +   
 Position +   
 Severity +  
 Triggered by +  

Exact Synonyms: Phenotypic modifier
Alternate IDs: HP:0000004
Definition Sources: HPO:probinson, UMLS:C4021064

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