Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the TMC1 gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Inheritance patterns describe how genetic conditions are passed from parents to children.
Age of onset indicates when symptoms typically first appear.
Inheritance patterns describe how genetic conditions are passed from parents to children.
Age of onset indicates when symptoms typically first appear.
The documentation surrounding autosomal dominant nonsyndromic hearing loss 36 is limited primarily due to its rarity and the recent identification of its genetic basis. As this condition affects a relatively small population, comprehensive clinical studies have not been extensively conducted. This can lead to feelings of isolation, but ongoing research may provide more insights in the future.
To navigate your journey with autosomal dominant nonsyndromic hearing loss 36, consider consulting an audiologist or a geneticist with expertise in hereditary hearing loss. Genetic counseling can provide valuable insights into the implications of the TMC1 mutation for you and your family. Although there are currently no patient organizations specifically for this condition, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can be helpful. Additionally, inquire about participation in any available clinical trials to stay informed about the latest research and treatment options.
Currently, there are no orphan drugs designated for autosomal dominant nonsyndromic hearing loss 36. However, there is one active clinical trial that may offer insights into potential treatments or management strategies. You can find more information about this trial by visiting ClinicalTrials.gov and searching for 'autosomal dominant nonsyndromic hearing loss 36'. This trial may provide opportunities for participation and contribute to the understanding of this condition.
Actionable guidance for navigating care for autosomal dominant nonsyndromic hearing loss 36
To navigate your journey with autosomal dominant nonsyndromic hearing loss 36, consider consulting an audiologist or a geneticist with expertise in hereditary hearing loss. Genetic counseling can provide valuable insights into the implications of the TMC1 mutation for you and your family. Although there are currently no patient organizations specifically for this condition, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can be helpful. Additionally, inquire about participation in any available clinical trials to stay informed about the latest research and treatment options.
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 6, 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.