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Ontology Browser

Parent Terms Term With Siblings Child Terms
Human phenotype +     
Biospecimen phenotypic feature +  
Blood group +  
Clinical modifier +   
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 +   
Past medical history +   
Phenotypic abnormality +   

Exact Synonyms: Phenotypic modifier
Alternate IDs: HP:0000004
Xrefs: UMLS:C4021064
Definition Sources:

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