ONTOLOGY REPORT - ANNOTATIONS


Term:Plummer-Vinson Syndrome
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Accession:DOID:9004304 term browser browse the term
Definition:A syndrome of DYSPHAGIA with IRON-DEFICIENCY ANEMIA that is due to congenital anomalies in the ESOPHAGUS (such as cervical esophageal webs). It is known as Patterson-Kelly syndrome in the United Kingdom.
Synonyms:exact_synonym: Kelly Syndrome;   Kelly's syndrome;   Kellys Syndrome;   Patterson Brown Kelly Syndrome;   Patterson Kelly Syndrome;   Patterson syndrome;   Patterson's Syndrome;   Pattersons Syndrome
 primary_id: MESH:D011004
 alt_id: RDO:0006364
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Plummer-Vinson Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rbbp8 RB binding protein 8, endonuclease JBrowse link 18 3,134,630 3,227,702 RGD:8554872

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  disease 14875
    syndrome 4220
      Plummer-Vinson Syndrome 1
Path 2
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  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        sensory system disease 4246
          Otorhinolaryngologic Diseases 1038
            Pharyngeal Diseases 157
              Deglutition Disorders 27
                dyskinesia of esophagus 20
                  Plummer-Vinson Syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.