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 3 89,715,022 89,753,455 RGD:1559268
RGD:8554872
RGD:7240710
RGD:13432090
G Chrnb2 cholinergic receptor, nicotinic, beta polypeptide 2 (neuronal) JBrowse link 3 89,753,448 89,764,632 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11726
    sensory system disease 4013
      skin disease 2113
        pigmentation disease 191
          dyschromatosis symmetrica hereditaria 2
Path 2
Term Annotations click to browse term
  disease 11726
    disease of anatomical entity 11187
      nervous system disease 8520
        sensory system disease 4013
          skin disease 2113
            pigmentation disease 191
              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.