Human Phenotype Ontology 
Grandparent Node:
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Sensorineural hearing impairment (HP:0000407)help
Parent Node:
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Childhood onset sensorineural hearing impairment (HP:0011474)help
..Starting node
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Postlingual sensorineural hearing impairment (HP:0008596)help
Term ID: 8596
Name: Postlingual sensorineural hearing impairment
Synonym:
Definition: A form of sensorineural hearing impairment with onset after the acquisition of speech.
Comments:
Reference: HP:0008596
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandInfantile sensorineural hearing impairment (HP:0008610) help
..expandPrelingual sensorineural hearing impairment (HP:0000399) 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:0008596HP:0008596Postlingual sensorineural hearing impairment0COCH CL E G H16902180OMIM:601369Deafness, autosomal dominant 9.46
HP:0008596HP:0008596Postlingual sensorineural hearing impairment0TIMM8A CL E G H167811817OMIM:304700Mohr-Tranebjaerg syndrome15
HP:0008596HP:0008596Postlingual sensorineural hearing impairment0TIMM8A CL E G H167811817ORPHA:52368Mohr-Tranebjaerg syndromeHP:0040282 - Frequent15


Genes (2) :COCH TIMM8A

Diseases (3) :OMIM:601369 OMIM:304700 ORPHA:52368
 

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