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
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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

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Term Annotations click to browse term
  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          hypotrichosis 12 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      nervous system disease 9154
        sensory system disease 4267
          skin disease 2270
            hair disease 214
              hypotrichosis 98
                hypotrichosis 12 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.