ONTOLOGY REPORT - ANNOTATIONS


Term:dyschromatosis symmetrica hereditaria
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Accession:DOID:0060257 term browser browse the term
Definition:A pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities. (DO)
Synonyms:exact_synonym: DSH;   DSH1;   Dyschromatosis Symmetrica Hereditaria 1;   Familial reticulate acropigmentation of Dohi;   RAD;   Reticulate acropigmentation of Dohi;   SYMMETRICAL DYSCHROMATOSIS OF EXTREMITIES;   Symmetric dyschromatosis of the extremities
 primary_id: MESH:C535729
 alt_id: OMIM:127400;   RDO:0001011
 xref: ORDO:41
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dyschromatosis symmetrica hereditaria term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Adar adenosine deaminase RNA specific JBrowse link NW_004936580 4,183,016 4,208,341 RGD:7240710
RGD:9068941
G Chrnb2 cholinergic receptor nicotinic beta 2 subunit JBrowse link NW_004936580 4,165,255 4,179,285 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 10652
    sensory system disease 3762
      skin disease 1969
        pigmentation disease 181
          dyschromatosis symmetrica hereditaria 2
Path 2
Term Annotations click to browse term
  disease 10652
    disease of anatomical entity 10186
      nervous system disease 7878
        sensory system disease 3762
          skin disease 1969
            pigmentation disease 181
              dyschromatosis symmetrica hereditaria 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.