Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the inner ear (HP:0000359)help
Parent Node:
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Morphological abnormality of the inner ear (HP:0011390)help
..Starting node
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Morphological abnormality of the nerves of the inner ear (HP:0011391)help
Term ID: 11391
Name: Morphological abnormality of the nerves of the inner ear
Synonym:
Definition:
Comments:
Reference: HP:0011391
Genes and Diseases:
 
       Child Nodes:
........expandAbnormality of the vestibular nerve (HP:0011392) help
................... HP:0011393 Aplasia of the vestibular nerve.
................... HP:0011394 Hypoplasia of the vestibular nerve
........expandAbnormality of the cochlear nerve (HP:0011396) help

 Sister Nodes: 
..expandAbnormal cochlea morphology (HP:0000375) help
..expandAbnormal inner ear epithelium morphology (HP:3000002) help
..expandAbnormality of the internal auditory canal (HP:0011384) help
..expandAplasia/Hypoplasia of the inner ear (HP:0008774) help
..expandMorphological abnormality of the vestibule of the inner ear (HP:0011376) 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:0011391HP:0011391Morphological abnormality of the nerves of the inner ear0 CL E G H
HP:0011391HP:0011396Abnormality of the cochlear nerve1 CL E G H
HP:0011391HP:0011392Abnormality of the vestibular nerve1 CL E G H
HP:0011391HP:0011394Hypoplasia of the vestibular nerve2 CL E G H
HP:0011391HP:0011393Aplasia of the vestibular nerve.2 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.