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ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 11
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Accession:DOID:0110708 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of SNRPE on chromosome 1q32.1. (DO)
Synonyms:exact_synonym: HYPT11
 primary_id: OMIM:615059
 alt_id: RDO:9000470
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hypotrichosis 11 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Snrpe small nuclear ribonucleoprotein polypeptide E JBrowse link 13 50,252,707 50,258,951 RGD:7240710
RGD:8554872

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Path 1
Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          hypotrichosis 11 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        sensory system disease 4249
          skin disease 2260
            hair disease 224
              hypotrichosis 108
                hypotrichosis 11 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.