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ONTOLOGY REPORT - ANNOTATIONS


Term:Deafness, Congenital Heart Defects, and Posterior Embryotoxon
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Accession:DOID:9008743 term browser browse the term
Synonyms:primary_id: MESH:C566604;   RDO:0014917
For additional species annotation, visit the Alliance of Genome Resources.


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Deafness, Congenital Heart Defects, and Posterior Embryotoxon term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Jag1 jagged canonical Notch ligand 1 JBrowse link 3 130,079,361 130,114,781 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15578
    Developmental Diseases 8717
      congenital heart disease 849
        Deafness, Congenital Heart Defects, and Posterior Embryotoxon 1
Path 2
Term Annotations click to browse term
  disease 15578
    disease of anatomical entity 14907
      nervous system disease 10189
        sensory system disease 4657
          Otorhinolaryngologic Diseases 1077
            auditory system disease 686
              Hearing Disorders 571
                Hearing Loss 567
                  Deafness, Congenital Heart Defects, and Posterior Embryotoxon 1
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.