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ONTOLOGY REPORT - ANNOTATIONS


Term:Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1
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Accession:DOID:9003089 term browser browse the term
Synonyms:exact_synonym: DFNA39-Dentinogenesis Imperfecta 1 Syndrome;   DFNA39/DGI1 SYNDROME
 narrow_synonym: Deafness, autosomal dominant nonsyndromic sensorineural 39, with dentinogenesis imperfecta 1
 primary_id: MESH:C565316
 alt_id: OMIM:605594;   RDO:0013990
For additional species annotation, visit the Alliance of Genome Resources.


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Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dspp dentin sialophosphoprotein JBrowse link 14 6,926,972 6,933,079 RGD:7240710
RGD:8554872
RGD:12910984

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    Stomatognathic Diseases 867
      tooth disease 238
        dentinogenesis imperfecta 8
          Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1 1
Path 2
Term Annotations click to browse term
  disease 15590
    disease of anatomical entity 14919
      nervous system disease 10196
        sensory system disease 4659
          Otorhinolaryngologic Diseases 1076
            auditory system disease 685
              Hearing Disorders 570
                Hearing Loss 566
                  Deafness 249
                    nonsyndromic deafness 150
                      autosomal dominant nonsyndromic deafness 49
                        Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.