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ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 4
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Accession:DOID:0110701 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of HR on chromosome 8p21.3. (DO)
Synonyms:exact_synonym: HYPT4;   Hypotrichosis, Marie Unna Type, 1;   Hypotrichosis, Marie Unna type;   MARIE UNNA HEREDITARY HYPOTRICHOSIS 1;   MUHH1;   Marie Unna congenital hypotrichosis;   Marie Unna hereditary hypotrichosis
 primary_id: MESH:C535912;   MESH:C567718
 alt_id: OMIM:146550;   RDO:0001280;   RDO:0015712
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hypotrichosis 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hr HR, lysine demethylase and nuclear receptor corepressor JBrowse link 15 52,241,801 52,261,276 RGD:7240710
RGD:8554872
RGD:11554173

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Path 1
Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          hypotrichosis 4 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        sensory system disease 4249
          skin disease 2260
            hair disease 224
              hypotrichosis 108
                hypotrichosis 4 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.