hearing loss disorder
MONDO:0005365Mondo
Findings
No curated finding names hearing loss disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A partial or complete loss of hearing in one or both ears. It is classified as conductive, sensory, or central.
Definition from the Mondo Disease Ontology (MONDO:0005365), read 2026-09-29. CC BY 4.0.
Genes
11 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- GJB2HGNC:4284
- Definitive · ClinGen · Autosomal dominant · 2018
- PNPT1HGNC:23166
- Definitive · G2P · Autosomal recessive · 2015
- FMN1HGNC:3768
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- SPATC1LHGNC:1298
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal dominant · 2018
- THOC1HGNC:19070
- Moderate · PanelApp Australia · Autosomal dominant · 2025
- FOXI1HGNC:3815
- Limited · ClinGen · Autosomal recessive · 2022
- GAS2HGNC:4167
- Limited · Ambry Genetics · Autosomal dominant · 2024
- IKZF2HGNC:13177
- Limited · Ambry Genetics · Autosomal dominant · 2025
- KCNQ4HGNC:6298
- Limited · Ambry Genetics · Autosomal recessive · 2025
- POLD3HGNC:20932
- Limited · Ambry Genetics · Autosomal dominant · 2025
- SIK3HGNC:29165
- Limited · Ambry Genetics · Autosomal dominant · 2025
Where it sits
- A kind of
- Narrower terms (11)
- auditory neuropathy
- central hearing loss
- conductive hearing loss disorder
- drug-induced hearing loss
- hearing loss, mixed conductive-sensorineural
- Johanson-Blizzard syndrome
- noise induced hearing loss
- nonsyndromic genetic hearing loss
- sensorineural hearing loss disorder
- sudden hearing loss disorder
- X-linked deafness
Other names
5 names
Resolves to: hearing loss disorder
- Also called
- hearing losshypoacuseshypoacusisloss of hearingloss, hearing