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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
For additional species annotation, visit the Alliance of Genome Resources.


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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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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          hypotrichosis 4 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        sensory system disease 4231
          skin disease 2240
            hair disease 201
              hypotrichosis 93
                hypotrichosis 4 1
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