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
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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 14823
    Pathological Conditions, Signs and Symptoms 7275
      Anatomical Pathological Conditions 1305
        Malformed Nails 19
          Congenital Deafness, and Onychodystrophy, Autosomal Dominant 1
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        sensory system disease 4244
          Otorhinolaryngologic Diseases 1038
            auditory system disease 662
              Hearing Disorders 551
                Hearing Loss 547
                  Deafness 262
                    Congenital Deafness, and Onychodystrophy, Autosomal Dominant 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.