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Human Disease
autosomal dominant nonsyndromic deafness 88
- Term ID
- DOID:0070611
- Synonyms
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- autosomal dominant deafness 88
- DFNA88
- Definition
- An autosomal dominant nonsyndromic deafness characterized by postlingual progressive severe sensorineural hearing loss with tinnitus that has_material_basis_in heterozygous mutation in the EPHA10 gene on chromosome 1p34. (2)
- References
- Ontology
- Human Disease ( DOID:0070611 )
- is a type of
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