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_004955545 1,078,319 1,106,938 RGD:9068941
RGD:7240710
G Chrnb2 cholinergic receptor nicotinic beta 2 subunit JBrowse link NW_004955545 1,065,457 1,077,056 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 10540
    sensory system disease 3700
      skin disease 1927
        pigmentation disease 174
          dyschromatosis symmetrica hereditaria 2
Path 2
Term Annotations click to browse term
  disease 10540
    disease of anatomical entity 10091
      nervous system disease 7755
        sensory system disease 3700
          skin disease 1927
            pigmentation disease 174
              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.