Human Phenotype Ontology 
Grandparent Node:
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Hearing impairment (HP:0000365)help
Parent Node:
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Conductive hearing impairment (HP:0000405)help
Parent Node:
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Mild hearing impairment (HP:0012712)help
..Starting node
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Mild conductive hearing impairment (HP:0008598)help
Term ID: 8598
Name: Mild conductive hearing impairment
Synonym: Conductive hearing loss, mild
Definition: A mild form of conductive hearing impairment.
Comments:
Reference: HP:0008598
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMild neurosensory hearing impairment (HP:0008587) help
..expandModerate conductive hearing impairment (HP:0012716) help
..expandSevere conductive hearing impairment (HP:0012717) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008598HP:0008598Mild conductive hearing impairment0CTSK CL E G H15132536ORPHA:763Pycnodysostosis39


Genes (1) :CTSK

Diseases (1) :ORPHA:763
 

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