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ONTOLOGY REPORT - ANNOTATIONS


Term:Sensorineural Deafness, Autosomal-Mitochondrial Type
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Accession:DOID:9000019 term browser browse the term
Synonyms:exact_synonym: Deafness, Nonsyndromic Sensorineural, Mitochondrial
 primary_id: MESH:C565637
 alt_id: OMIM:500008;   RDO:0014221
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Sensorineural Deafness, Autosomal-Mitochondrial Type 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:11554173
RGD:8554872
G Mt-nd1 mitochondrially encoded NADH dehydrogenase 1 JBrowse link MT 2,740 3,694 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15620
    sensory system disease 4681
      auditory system disease 684
        inner ear disease 495
          sensorineural hearing loss 459
            Sensorineural Deafness, Autosomal-Mitochondrial Type 2
Path 2
Term Annotations click to browse term
  disease 15620
    disease of anatomical entity 14949
      nervous system disease 10219
        sensory system disease 4681
          Otorhinolaryngologic Diseases 1075
            auditory system disease 684
              Hearing Disorders 569
                Hearing Loss 565
                  sensorineural hearing loss 459
                    Sensorineural Deafness, Autosomal-Mitochondrial Type 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.