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Human Disease
autosomal dominant nonsyndromic deafness 12
- Term ID
- DOID:0110544
- Synonyms
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- autosomal dominant deafness 12
- autosomal dominant deafness 8
- DFNA12
- DFNA8
- Definition
- An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23. https://www.ncbi.nlm.nih.gov/pubmed/9590290
- References
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- ICD10CM:H90.3
- MIM:601543
- Ontology
- Human Disease ( DOID:0110544 )
- is a type of
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Genes Involved
Zebrafish Models