hearing loss, autosomal recessive 107

Rare Disease

MONDO:0033199

Also known as:

DFNB107autosomal recessive nonsyndromic deafness 107deafness, autosomal recessive 107

Genes

Clinical Trials

–

Newborn Screening

–

Patient Groups

–

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Report Generation Failed

We couldn't automatically generate the report. This may be due to temporary service issues.

Need this data in your product?

Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.

Explore API Start Free

← Back to All Diseases

hearing loss, autosomal recessive 107

Patient-Friendly Information

Need this data in your product?

Scientific Intelligence