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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:Amyloidosis
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Accession:HP:0011034 term browser browse the term
Definition:The presence of amyloid deposition in one or more tissues. Amyloidosis may be defined as the extracellular deposition of amyloid in one or more sites of the body.
Comment:The medical literautre on amyloidosis is confused with clinical and histochemical designations used when the amyloid disease processes were poorly understood. To be designated an amyloid fibril protein, the protein must occur in tissue deposits and exhibit affinity for Congo red and green birefringence when viewed by polarization microscopy.
Synonyms:exact_synonym: Amyloid disease
 xref: EFO:1001875;   SNOMEDCT_US:17602002;   UMLS:C0002726


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  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of metabolism/homeostasis 0
        Amyloidosis 0
          AA amyloidosis 0
          Amyloid goiter 0
          Amyloidosis of peripheral nerves 0
          Cardiac amyloidosis + 0
          Cerebral amyloid angiopathy 0
          Conjunctival amyloidosis 0
          Corneal amyloidosis 0
          Cutaneous amyloidosis + 0
          Generalized amyloid deposition 0
          Hepatic amyloidosis 0
          Positive serum amyloid P scintigraphy 0
          Pulmonary amyloidosis 0
          Renal amyloidosis + 0
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