sensorineural hearing loss disorder
MONDO:0020678Mondo
Findings
No curated finding names sensorineural hearing loss disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Hearing loss in which the root cause lies in the inner ear or sensory organ (cochlea and associated structures) or the vestibulocochlear nerve (cranial nerve VIII).
Definition from the Mondo Disease Ontology (MONDO:0020678), read 2026-09-29. CC BY 4.0.
Genes
5 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.
- OXR1HGNC:15822
- Strong · PanelApp Australia · Autosomal recessive · 2025
- PKHD1L1HGNC:20313
- Strong · PanelApp Australia · Autosomal recessive · 2025
- ANKRD24HGNC:29424
- Moderate · LiferaOmics · Autosomal recessive · 2026
- Limited · Ambry Genetics · Autosomal recessive · 2025
- Limited · PanelApp Australia · Autosomal recessive · 2025
- FOXF2HGNC:3810
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- THOC1HGNC:19070
- Limited · Ambry Genetics · Autosomal dominant · 2020
Where it sits
- A kind of
- Narrower terms (3)
Other names
3 names
Resolves to: sensorineural hearing loss disorder
- Also called
- sensorineural deafnesssensorineural hearing lossSNHL