ONTOLOGY REPORT - ANNOTATIONS


Term:Deafness, with Smith-Magenis Syndrome
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Accession:DOID:9007233 term browser browse the term
Synonyms:primary_id: RDO:9000633
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Deafness, with Smith-Magenis Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Myo15a myosin XVA JBrowse link 10 46,840,098 46,897,362 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    syndrome 4220
      Deafness, with Smith-Magenis Syndrome 1
Path 2
Term Annotations click to browse term
  disease 14875
    Pathological Conditions, Signs and Symptoms 7362
      Pathologic Processes 4865
        Chromosome Aberrations 519
          Aneuploidy 426
            Monosomy 381
              Chromosome Deletion 381
                chromosomal deletion syndrome 325
                  Smith-Magenis syndrome 35
                    Deafness, with Smith-Magenis Syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.