Human Phenotype Ontology 
..Starting node
..expandClinical relevance (HP:0045088)help
Term ID: 45088
Name: Clinical relevance
Synonym:
Definition: Subontology for annotating phenotypic features as distinctive or minor findings in patients. The subontology is intended to be used to annotate subjective clinical impressions of whether a certain finding is important for the differential diagnosis.
Comments:
Reference: HP:0045088
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0045088HP:0045088Clinical relevance0 CL E G H
HP:0045088HP:0045090Minor finding1 CL E G H
HP:0045088HP:0045089Distinctive finding1 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.