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Human Disease
autosomal dominant nonsyndromic deafness 79
- Term ID
- DOID:0112160
- Synonyms
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- DFNA79
- Definition
- An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SCD5 gene on chromosome 4q21.22. https://pubmed.ncbi.nlm.nih.gov/31972369/
- References
- Ontology
- Human Disease ( DOID:0112160 )
- is a type of
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