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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
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


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Path 1
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  disease 21128
    syndrome 10833
      Plummer-Vinson Syndrome 0
Path 2
Term Annotations click to browse term
  disease 21128
    disease of anatomical entity 18211
      nervous system disease 14059
        Neurologic Manifestations 10039
          sensory system disease 6940
            Otorhinolaryngologic Diseases 1735
              Pharyngeal Diseases 268
                Deglutition Disorders 85
                  dyskinesia of esophagus 75
                    Plummer-Vinson Syndrome 0
paths to the root