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Human Disease
autosomal dominant nonsyndromic deafness 15
- Term ID
- DOID:0110546
- Synonyms
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- autosomal dominant deafness 15
- autosomal dominant nonsyndromic deafness 52
- DFNA15
- Definition
- An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32. (2)
- References
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- ICD10CM:H90.3
- MIM:602459
- Ontology
- Human Disease ( DOID:0110546 )
- is a type of
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Zebrafish Models