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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
For additional species annotation, visit the Alliance of Genome Resources.


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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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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          hypotrichosis 11 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 11 1
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