ONTOLOGY REPORT - ANNOTATIONS


Term:dyschromatosis universalis hereditaria
go back to main search page
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.


show annotations for term's descendants       view all columns           Sort by:
 
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
G Sash1 SAM and SH3 domain containing 1 JBrowse link 1 2,782,905 2,950,749 RGD:13592920
Dyschromatosis Universalis Hereditaria 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sash1 SAM and SH3 domain containing 1 JBrowse link 1 2,782,905 2,950,749 RGD:7240710
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 14875
    sensory system disease 4246
      skin disease 2253
        pigmentation disease 212
          dyschromatosis universalis hereditaria 2
            Dyschromatosis Universalis Hereditaria 1 1
            Dyschromatosis Universalis Hereditaria 2 0
            Dyschromatosis Universalis Hereditaria 3 1
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        sensory system disease 4246
          skin disease 2253
            pigmentation disease 212
              dyschromatosis universalis hereditaria 2
                Dyschromatosis Universalis Hereditaria 1 1
                Dyschromatosis Universalis Hereditaria 2 0
                Dyschromatosis Universalis Hereditaria 3 1
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.