Preferred Name |
amyloidosis |
|
Synonyms |
amyloid disease |
|
Definitions |
An acquired metabolic disease that has_material_basis_in extracellular tissue deposition of mis-folded proteins called fibrils composed of low molecular weight subunits of a variety of proteins. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition. |
|
ID |
http://purl.obolibrary.org/obo/DOID_9120 |
|
database_cross_reference |
ICD10CM:E85 ICD9CM:277.3 SNOMEDCT_US_2020_03_01:154769007 UMLS_CUI:C0002726 MESH:D000686 NCI:C2868 |
|
has exact match |
MESH:D000686 |
|
has exact synonym |
amyloid disease |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:9120 |
|
imported from | ||
in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/doid#NCIthesaurus http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_FlyBase_slim |
|
label |
amyloidosis |
|
notation |
DOID:9120 |
|
prefLabel |
amyloidosis |
|
textual definition |
An acquired metabolic disease that has_material_basis_in extracellular tissue deposition of mis-folded proteins called fibrils composed of low molecular weight subunits of a variety of proteins. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition. |
|
subClassOf |
The BioAssay Ontology integrates with OntoloBridge, allowing community users to suggest additions to the public ontology. Complete the template below to submit a term request directly to the ontology maintainer.
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Example: Involves the use of a tissue derived from a living organism and is a heterogeneous assay type.
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