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ONTOLOGY REPORT - ANNOTATIONS


Term:Congenital Deafness, and Onychodystrophy, Autosomal Dominant
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Accession:DOID:9006023 term browser browse the term
Synonyms:exact_synonym: DDOD;   DDOD SYNDROME;   DEAFNESS, CONGENITAL, WITH ONYCHODYSTROPHY, AUTOSOMAL DOMINANT
 primary_id: MESH:C567274;   RDO:0015390
 alt_id: OMIM:124480
For additional species annotation, visit the Alliance of Genome Resources.


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Congenital Deafness, and Onychodystrophy, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Atp6v1b2 ATPase H+ transporting V1 subunit B2 JBrowse link 16 22,326,537 22,350,143 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    Pathological Conditions, Signs and Symptoms 8013
      Anatomical Pathological Conditions 1323
        Malformed Nails 20
          Congenital Deafness, and Onychodystrophy, Autosomal Dominant 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
                    Congenital Deafness, and Onychodystrophy, Autosomal Dominant 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.