Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 97

Term ID
DOID:0110539
Synonyms
  • autosomal recessive deafness 97
  • DFNB97
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MET gene on chromosome 7q31. https://www.ncbi.nlm.nih.gov/pubmed/25941349
References
Ontology
Human Disease   ( DOID:0110539 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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