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Descriptor English: | Amyloidosis | ||||
Descriptor Spanish: |
Amiloidosis
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Descriptor Portuguese: | Amiloidose | ||||
Descriptor French: | Amyloïdose | ||||
Entry term(s): |
Amylose (maladie) |
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Tree number(s): |
C18.452.845.500 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000686 | ||||
Scope note: | A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. |
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Annotation: | coord IM with organ/dis precoord (IM); /genet: consider also AMYLOIDOSIS, HEREDITARY |
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Allowable Qualifiers: |
BL sang CF liquide cérébrospinal CI induit chimiquement CL classification CN congénital CO complications DG imagerie diagnostique DH diétothérapie DI diagnostic DT traitement médicamenteux EC économie EH ethnologie EM embryologie EN enzymologie EP épidémiologie ET étiologie GE génétique HI histoire IM immunologie ME métabolisme MI microbiologie MO mortalité NU soins infirmiers PA anatomopathologie PC prévention et contrôle PP physiopathologie PS parasitologie PX psychologie RH rééducation et réadaptation RT radiothérapie SU chirurgie TH thérapie UR urine VE médecine vétérinaire VI virologie |
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Related: |
Amyloïde
MeSH Paraprotéinémies MeSH Syndromes lymphoprolifératifs MeSH | ||||
DeCS ID: | 699 | ||||
Unique ID: | D000686 | ||||
NLM Classification: | WD 205.5.A6 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 1966/01/01 | ||||
Date of Entry: | 1999/01/01 | ||||
Revision Date: | 2009/07/06 |
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Amyloïdose
- Preferred
Concept UI |
M0001053 |
Preferred term | Amyloïdose |
Entry term(s) |
Amylose (maladie) |
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