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A disease characterized by hearing loss that is not part of a larger syndrome.
Features include common findings: Prelingual sensorineural hearing impairment, Progressive sensorineural hearing impairment, Delayed speech and language development, and Abnormal speech discrimination and others; and sometimes findings: Conductive hearing impairment, High-frequency hearing impairment, Abnormal vestibulo-ocular reflex, and Childhood onset sensorineural hearing impairment and others. 13 total HPO annotations.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Ears | 11 |
Biomarker and diagnostic research for nonsyndromic genetic hearing loss has been reported in the published literature.
Phenotype severity distribution: 6 common features.
Estimated prevalence: Unknown (Unknown prevalence).
1 clinical trial registered. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.
128 publications have been identified in PubMed for nonsyndromic genetic hearing loss. Research spans Basic Science / Preclinical (39%), Case Report / Case Series (27%), and Epidemiology / Natural History (16%).
Research Type | Count | % of Total |
|---|---|---|
Laboratory research | 50 | 39% |
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 4:31 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Prelingual sensorineural hearing impairment, Progressive sensorineural hearing impairment, Postlingual sensorineural hearing impairment
Brain and nerves | 2 | Delayed speech and language development, Abnormal speech discrimination |
Eyes | 1 | Abnormal vestibulo-ocular reflex |
Patient case studies |
34 |
27% |
Disease patterns and progression | 21 | 16% |
Research summaries | 9 | 7% |
New treatment approaches | 7 | 5% |
Testing and diagnosis research | 6 | 5% |
Other research | 1 | 1% |
Chen R (2026). [PMID: 41078281](https://pubmed.ncbi.nlm.nih.gov/41078281/). *American journal of medical genetics. Part A*. [Case Report / Case Series]
Abghari FZ (2026). [PMID: 42231373](https://pubmed.ncbi.nlm.nih.gov/42231373/). *BMC Med Genomics*. [Basic Science / Preclinical]
Morris JA (2026). [PMID: 41516362](https://pubmed.ncbi.nlm.nih.gov/41516362/). *International journal of molecular sciences*. [Review / Meta-Analysis]
Lian J (2026). [PMID: 41726133](https://pubmed.ncbi.nlm.nih.gov/41726133/). *Open medicine (Warsaw, Poland)*. [Case Report / Case Series]
Jang SH (2026). [PMID: 41058175](https://pubmed.ncbi.nlm.nih.gov/41058175/). *Molecular therapy : the journal of the American Society of Gene Therapy*. [Case Report / Case Series]
Kutija Fučkar I (2026). [PMID: 42074586](https://pubmed.ncbi.nlm.nih.gov/42074586/). *Genes (Basel)*. [Epidemiology / Natural History]
Xiao Y (2026). [PMID: 41833579](https://pubmed.ncbi.nlm.nih.gov/41833579/). *EBioMedicine*. [Case Report / Case Series]
Li S (2026). [PMID: 41945437](https://pubmed.ncbi.nlm.nih.gov/41945437/). *Proc Natl Acad Sci U S A*. [Basic Science / Preclinical]
Hua MW (2026). [PMID: 41189051](https://pubmed.ncbi.nlm.nih.gov/41189051/). *Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology*. [Basic Science / Preclinical]
DeSollar B (2026). [PMID: 41979979](https://pubmed.ncbi.nlm.nih.gov/41979979/). *JMIR Bioinform Biotechnol*. [Case Report / Case Series]