Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene.
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 6, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 6, 2026
The documentation for autosomal dominant nonsyndromic hearing loss 11 is limited primarily due to its rarity and the recent identification of the MYO7A gene as a causative factor. Conditions like this often lack comprehensive clinical studies because they affect fewer individuals, making it challenging to gather extensive data on clinical features and treatment options.
To navigate your condition effectively, consider consulting an audiologist or an otolaryngologist (ENT specialist) with experience in genetic hearing loss. Genetic counseling can also be beneficial, as it provides insights into the inheritance pattern and implications for family members. For more resources, visit the Genetic and Rare Diseases Information Center at rarediseases.info.nih.gov. Additionally, inquire about any available natural history studies that may provide further understanding of the condition.
Currently, there is one active clinical trial related to autosomal dominant nonsyndromic hearing loss 11. You can find more information about ongoing research and potential participation opportunities by visiting ClinicalTrials.gov. This trial may offer insights into the condition and potential future therapies, providing hope for affected individuals.
Actionable guidance for navigating care for autosomal dominant nonsyndromic hearing loss 11
To navigate your condition effectively, consider consulting an audiologist or an otolaryngologist (ENT specialist) with experience in genetic hearing loss. Genetic counseling can also be beneficial, as it provides insights into the inheritance pattern and implications for family members. For more resources, visit the Genetic and Rare Diseases Information Center at rarediseases.info.nih.gov. Additionally, inquire about any available natural history studies that may provide further understanding of the condition.
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.
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.