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Human Disease
autosomal dominant nonsyndromic deafness 56
- Term ID
- DOID:0110581
- Synonyms
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- autosomal dominant deafness 56
- DFNA56
- Definition
- An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TNC gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/23936043
- References
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- ICD10CM:H90.3
- MIM:615629
- Ontology
- Human Disease ( DOID:0110581 )
- is a type of
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