ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 2
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Accession:DOID:0110699 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of CDSN on chromosome 6p21.33. (DO)
Synonyms:exact_synonym: HTSS;   HTSS1;   HYPT2;   hypotrichosis simplex of scalp;   hypotrichosis simplex of the scalp 1;   hypotrichosis, Spanish type
 primary_id: MESH:C564143
 alt_id: OMIM:146520;   RDO:0008026;   RDO:0013197
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hypotrichosis 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cdsn corneodesmosin JBrowse link 17 35,543,082 35,557,180 RGD:7240710
RGD:8554872

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Path 1
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  disease 11832
    Developmental Diseases 7524
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6844
        genetic disease 6228
          hypotrichosis 2 1
Path 2
Term Annotations click to browse term
  disease 11832
    disease of anatomical entity 11283
      nervous system disease 8564
        sensory system disease 4038
          skin disease 2129
            hair disease 212
              hypotrichosis 96
                hypotrichosis 2 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.