ONTOLOGY REPORT - ANNOTATIONS


Term:autosomal dominant nonsyndromic deafness 17
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Accession:DOID:0110548 term browser browse the term
Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYH9 gene on chromosome 22q12. (DO)
Synonyms:exact_synonym: DFNA17;   Late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration;   autosomal dominant deafness 17;   deafness, autosomal dominant nonsyndromic sensorineural 17
 narrow_synonym: COCHLEOSACCULAR DEGENERATION
 primary_id: MESH:C538050
 alt_id: OMIM:603622;   RDO:0003984
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autosomal dominant nonsyndromic deafness 17 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Myh9 myosin, heavy chain 9 JBrowse link 7 118,740,005 118,792,507 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14920
    sensory system disease 4265
      auditory system disease 667
        inner ear disease 473
          sensorineural hearing loss 437
            MYH-9 related disease 1
              autosomal dominant nonsyndromic deafness 17 1
Path 2
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      nervous system disease 9150
        sensory system disease 4265
          Otorhinolaryngologic Diseases 1042
            auditory system disease 667
              Hearing Disorders 553
                Hearing Loss 549
                  Deafness 261
                    nonsyndromic deafness 156
                      autosomal dominant nonsyndromic deafness 51
                        autosomal dominant nonsyndromic deafness 17 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.