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Human Disease

autosomal recessive nonsyndromic deafness 38

Term ID
DOID:0110496
Synonyms
  • autosomal recessive deafness 38
  • DFNB38
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6q26-q27. https://www.ncbi.nlm.nih.gov/pubmed/12890929
References
Ontology
Human Disease   ( DOID:0110496 )
Relationships
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Genes Involved
Zebrafish Models
Citations