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ONTOLOGY REPORT - ANNOTATIONS


Term:mitochondrial nonsyndromic sensorineural deafness
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Accession:DOID:0111751 term browser browse the term
Definition:A sensorineural hearing loss that has_material_basis_in mutation in one of several different mitochondrial genes including; MTRNR1, MTTS1, MTCO1, MTTH, MTND1, and MTTI. (DO)
Synonyms:exact_synonym: mitochondrially inherited nonsyndromic sensorineural deafness
 primary_id: OMIM:500008
 xref: NCI:C148321
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mitochondrial nonsyndromic sensorineural deafness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mt-co1 mitochondrially encoded cytochrome c oxidase I JBrowse link MT 5,323 6,867 RGD:8554872
RGD:13592920
G Mt-nd1 mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 JBrowse link MT 2,740 3,694 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15849
    sensory system disease 4942
      auditory system disease 687
        inner ear disease 501
          sensorineural hearing loss 464
            Nonsyndromic Sensorineural Hearing Loss 24
              mitochondrial nonsyndromic sensorineural deafness 2
Path 2
Term Annotations click to browse term
  disease 15849
    disease of anatomical entity 15241
      nervous system disease 10711
        sensory system disease 4942
          Otorhinolaryngologic Diseases 1092
            auditory system disease 687
              Hearing Disorders 572
                Hearing Loss 568
                  sensorineural hearing loss 464
                    Nonsyndromic Sensorineural Hearing Loss 24
                      mitochondrial nonsyndromic sensorineural deafness 2
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.