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ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 13
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Accession:DOID:0110710 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of KRT71 on chromosome 12q13.13. (DO)
Synonyms:exact_synonym: HYPT13;   hypotrichosis with woolly hair
 primary_id: OMIM:615896
 alt_id: RDO:9001603
For additional species annotation, visit the Alliance of Genome Resources.


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hypotrichosis 13 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Krt71 keratin 71 JBrowse link 7 143,345,201 143,371,346 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15984
    sensory system disease 4970
      skin disease 2649
        hair disease 231
          hypotrichosis 112
            hypotrichosis 13 1
Path 2
Term Annotations click to browse term
  disease 15984
    Developmental Diseases 9281
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8095
        genetic disease 7613
          monogenic disease 5382
            autosomal genetic disease 4348
              autosomal dominant disease 2713
                hypotrichosis 13 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.