loading...| Preferred Name | Amyloidosis | |
| Synonyms |
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| Definitions |
The presence of `amyloid deposition` (MPATH:34) in one or more tissues. Amyloidosis may be defined as the extracellular deposition of amyloid in one or more sites of the body. 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 polarisation microscopy. |
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| ID |
http://purl.obolibrary.org/obo/HP_0011034 |
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| 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 polarisation microscopy. |
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| created_by |
peter |
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| creation_date |
2011-03-06T10:56:39Z |
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| database_cross_reference |
MeSH:D000686 |
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| definition |
The presence of `amyloid deposition` (MPATH:34) in one or more tissues. Amyloidosis may be defined as the extracellular deposition of amyloid in one or more sites of the body. |
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| has_obo_namespace |
human_phenotype |
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| id |
HP:0011034 |
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| imported from | ||
| label |
Amyloidosis |
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| manifests_in |
http://purl.obolibrary.org/obo/DOID_9352 |
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| namespace |
obo |
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| notation |
HP:0011034 |
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| prefLabel |
Amyloidosis |
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| subClassOf |