FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term sensorineural hearing loss ID (Ontology) DOID:10003 (Human Disease)
Definition An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem.
Also Known As "central hearing loss" ; "High frequency deafness" ; "High Frequency Hearing Loss" (for all, see Synonyms field below)
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Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      10
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 sensorineural hearing loss      11     11
 exacerbates | sensorineural hearing loss       2       --
 model of | sensorineural hearing loss      11       --
Spanning Tree (Parents/Children)
Only view relationship: 
  auditory system disease
   |__inner ear disease
       |__sensorineural hearing loss  22 rec.
           |__autosomal-mitochondrial sensorineural deafness
           |__mitochondrial nonsyndromic sensorineural deafness
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Is a inner ear disease
Part of
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Synonyms
  • "central hearing loss" EXACT
    "High frequency deafness" EXACT
    "High Frequency Hearing Loss" EXACT
    "high-frequency hearing loss" EXACT
    "Perceptive deafness" EXACT
    "Perceptive hearing loss" EXACT
    "Perceptive hearing loss or deafness" EXACT
    "Sensorineural Deafness" EXACT
    "Sensory hearing loss" EXACT
Secondary IDs
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ICD10CM:H90.5
ICD9CM:389.1
MESH:D006319
NCI:C26739
SNOMEDCT_US_2023_03_01:60700002
UMLS_CUI:C0018784