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Human Disease

autosomal recessive nonsyndromic deafness 7

Term ID
DOID:0110520
Synonyms
  • autosomal recessive deafness 7
  • DFNB11
  • DFNB7
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21. https://www.ncbi.nlm.nih.gov/pubmed/11850618
References
Ontology
Human Disease   ( DOID:0110520 )
Relationships
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Genes Involved
Zebrafish Models