An autosomal recessive nonsyndromic deafness that has material basis in variation between D7S554 and D7S2459 in the chromosome region 7q31.
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
The documentation for autosomal recessive nonsyndromic hearing loss 14 is limited due to its rarity and the lack of systematic clinical studies. Because this condition affects a small number of individuals, comprehensive data collection and characterization have been challenging. Additionally, the genetic basis is still being investigated, which contributes to the gaps in clinical knowledge.
To navigate your care effectively, consider seeking a specialist in genetics or a genetic counselor who has experience with hereditary hearing loss. They can provide insights into potential genetic testing options and family planning considerations. Additionally, while there are currently no patient organizations specifically for this condition, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can offer valuable information and support. Participating in clinical trials may also be an option to explore for gaining access to new treatment approaches.
Currently, there is one active clinical trial related to autosomal recessive nonsyndromic hearing loss 14. This trial may provide insights into potential treatment approaches or further understanding of the condition. For more information on ongoing studies, you can visit the ClinicalTrials.gov search page at https://clinicaltrials.gov/search?cond=autosomal%20recessive%20nonsyndromic%20hearing%20loss%2014.
Actionable guidance for navigating care for autosomal recessive nonsyndromic hearing loss 14
To navigate your care effectively, consider seeking a specialist in genetics or a genetic counselor who has experience with hereditary hearing loss. They can provide insights into potential genetic testing options and family planning considerations. Additionally, while there are currently no patient organizations specifically for this condition, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can offer valuable information and support. Participating in clinical trials may also be an option to explore for gaining access to new treatment approaches.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Inheritance patterns describe how genetic conditions are passed from parents to children.
Age of onset indicates when symptoms typically first appear.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.