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HUMAN PHENOTYPE - ANNOTATIONS

The Human Phenotype Ontology (HPO) is downloaded weekly from http://compbio.charite.de/hudson/job/hpo/lastStableBuild/artifact/ontology/release/hp.obo. The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at http://www.human-phenotype-ontology.org/.
Term:Celiac disease
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Accession:HP:0002608 term browser browse the term
Definition:Celiac disease (CD) is an autoimmune condition affecting the small intestine, triggered by the ingestion of gluten, the protein fraction of wheat, barley, and rye. Clinical manifestations of CD are highly variable and include both gastrointestinal and non-gastrointestinal features. The hallmark of CD is an immune-mediated enteropathy. This term is included because the occurrence of CD is seen as a feature of a number of other diseases.
Synonyms:exact_synonym: Celiac sprue;   Coeliac disease;   Coeliac sprue
 narrow_synonym: refractory celiac disease
 xref: EFO:0001060;   EFO:0009266;   SNOMEDCT_US:396331005;   UMLS:C0007570


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Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the immune system 0
        Abnormality of immune system physiology 0
          Immunologic hypersensitivity 0
            Celiac disease 0
Path 2
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the digestive system 0
        Abnormality of the gastrointestinal tract 0
          Abnormal gastrointestinal tract morphology 0
            Abnormal intestine morphology 0
              Abnormal small intestine morphology 0
                Celiac disease 0
paths to the root