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Human Disease

autosomal recessive nonsyndromic deafness 2

Term ID
DOID:0110477
Synonyms
  • autosomal recessive deafness 2
  • DFNB2
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MYO7A gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/9171833
References
Ontology
Human Disease   ( DOID:0110477 )
Relationships
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Genes Involved
Zebrafish Models