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Human Disease
autosomal dominant nonsyndromic deafness 65
- Term ID
- DOID:0110586
- Synonyms
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- autosomal dominant deafness 65
- DFNA65
- Definition
- An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13. (2)
- References
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- ICD10CM:H90.3
- MIM:616044
- Ontology
- Human Disease ( DOID:0110586 )
- is a type of
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