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ONTOLOGY REPORT - ANNOTATIONS


Term:dyschromatosis universalis hereditaria
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Accession:DOID:0060304 term browser browse the term
Definition:A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution. (DO)
Synonyms:primary_id: MESH:C535730
 alt_id: RDO:0001012
 xref: GARD:1996;   OMIM:PS127500;   ORDO:241
For additional species annotation, visit the Alliance of Genome Resources.


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dyschromatosis universalis hereditaria term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcb6 ATP binding cassette subfamily B member 6 JBrowse link 9 82,373,950 82,382,228 RGD:13592920
Dyschromatosis Universalis Hereditaria 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcb6 ATP binding cassette subfamily B member 6 JBrowse link 9 82,373,950 82,382,228 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    sensory system disease 4231
      skin disease 2240
        pigmentation disease 210
          dyschromatosis universalis hereditaria 1
            Dyschromatosis Universalis Hereditaria 1 0
            Dyschromatosis Universalis Hereditaria 2 0
            Dyschromatosis Universalis Hereditaria 3 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        sensory system disease 4231
          skin disease 2240
            pigmentation disease 210
              dyschromatosis universalis hereditaria 1
                Dyschromatosis Universalis Hereditaria 1 0
                Dyschromatosis Universalis Hereditaria 2 0
                Dyschromatosis Universalis Hereditaria 3 1
paths to the root