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Human Disease

autosomal recessive nonsyndromic deafness 86

Term ID
DOID:0110532
Synonyms
  • autosomal recessive deafness 86
  • DFNB86
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/24387994
References
Ontology
Human Disease   ( DOID:0110532 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations