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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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15992
    sensory system disease 4969
      skin disease 2651
        hair disease 231
          hypotrichosis 112
            hypotrichosis 12 1
Path 2
Term Annotations click to browse term
  disease 15992
    Developmental Diseases 9280
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8094
        genetic disease 7612
          monogenic disease 5382
            autosomal genetic disease 4347
              autosomal dominant disease 2713
                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.