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Human Disease

autosomal dominant nonsyndromic deafness 87

Term ID
DOID:0070606
Synonyms
  • autosomal dominant deafness 87
  • DFNA87
Definition
An autosomal dominant nonsyndromic deafness characterized by prelingual profound sensorineural hearing loss with inner ear anomalies, including cochlear maldevelopment, absence of the osseous spiral lamina, and/or an enlarged vestibular aqueduct that has_material_basis_in heterozygous mutation in the PI4KB gene on chromosome 1q21. https://pubmed.ncbi.nlm.nih.gov/33358777/
References
Ontology
Human Disease   ( DOID:0070606 )
Relationships
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Genes Involved
Zebrafish Models