ONKI3 | Medical Subject Headings

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Amyloidosis 17 coordinate concepts 3 subordinate concepts ∟ Amyloid Neuropathies \| ∟ Amyloidosis, Familial \| ∟ Cerebral Amyloid Angiopathy ∟ Acid-Base Imbalance \| ∟ Brain Diseases, Metabolic \| ∟ Calcium Metabolism Disorders \| ∟ D008659Q000151* \| ∟ DNA Repair-Deficiency Disorders \| ∟ Glucose Metabolism Disorders \| ∟ Iron Metabolism Disorders \| ∟ Lipid Metabolism Disorders \| ∟ Malabsorption Syndromes \| ∟ Metabolic Syndrome X \| ∟ Metabolism, Inborn Errors \| ∟ Mitochondrial Diseases \| ∟ Phosphorus Metabolism Disorders \| ∟ Porphyrias \| ∟ Skin Diseases, Metabolic \| ∟ Wasting Syndrome \| ∟ Water-Electrolyte Imbalance X
Broader terms:	Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Amyloidosis Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Amyloid Neuropathies \| Amyloidosis, Familial \| Cerebral Amyloid Angiopathy X
Annotation:	coord IM with organ/dis precoord (IM); /genet: consider also AMYLOIDOSIS, HEREDITARY X
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. X
activeMeSHYear*:	2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	2004-07-07X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Related term:	Amyloid \| Lymphoproliferative Disorders \| Paraproteinemias X
Type:	Concept X
Coordinate terms:	Acid-Base Imbalance \| Brain Diseases, Metabolic \| Calcium Metabolism Disorders \| D008659Q000151* \| DNA Repair-Deficiency Disorders \| Glucose Metabolism Disorders \| Iron Metabolism Disorders \| Lipid Metabolism Disorders \| Malabsorption Syndromes \| Metabolic Syndrome X \| Metabolism, Inborn Errors \| Mitochondrial Diseases \| Phosphorus Metabolism Disorders \| Porphyrias \| Skin Diseases, Metabolic \| Wasting Syndrome \| Water-Electrolyte Imbalance X
URI:	X
Labels and equivalent concepts:	Amyloidoosi (fi) Amyloiditauti (fi, replaced) Amyloidirappeuma (fi, replaced) Amyloidin kertyminen (fi, replaced) Amyloidos (sv) Amyloidosis (la-FI, replaced) X
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