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ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 12
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Accession:DOID:0110709 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of RPL21 on chromosome 13q12.2. (DO)
Synonyms:exact_synonym: HYPT12
 primary_id: OMIM:615885
 alt_id: RDO:9001602
For additional species annotation, visit the Alliance of Genome Resources.


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hypotrichosis 12 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rpl21 ribosomal protein L21 JBrowse link 12 9,996,919 9,999,998 RGD:8554872
RGD:7240710

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Term Annotations click to browse term
  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          hypotrichosis 12 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 12 1
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