68790008: Amyloid deposition (morphologic abnormality)

SNOMED CT Concept\Body structure\Body structure, altered from its original anatomical structure (morphologic abnormality)\Morphologically abnormal structure\Deposition\Amyloid deposition

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Amyloid deposition	Is a	Deposition	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial localized cutaneous amyloidosis (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some
Secondary localized cutaneous amyloidosis (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some
Systemic amyloidosis affecting skin (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some
Amyloidosis limited to skin (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some
Lattice corneal dystrophy (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Amyloidosis of spleen	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Ocular amyloid deposit	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Lattice corneal dystrophy Type I (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
dystrophia corneae latticis type 2	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
dystrophia corneae latticis type 2	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
familliær amyloid polyneuropati, type V	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
dystrophia corneae latticis type 3	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Gelatinous droplike corneal dystrophy (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
dystrophia corneae latticis type 2	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
dystrophia corneae latticis type 2	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
dystrophia corneae latticis type 2	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
dystrophia corneae latticis type 2	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	3
Amyloid light-chain nephropathy (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Familial visceral amyloidosis, Ostertag type	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
AA amyloid nephropathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Familial amyloid nephropathy with urticaria AND deafness	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Amyloid nephropathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Familial visceral amyloidosis, Ostertag type	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Amyloid disease of the urethra	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Isolated atrial amyloid	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Primary familial amyloid myopathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Ocular amyloid deposit	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Conjunctival amyloidosis	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Primary sporadic amyloid myopathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Amyloid polyneuropathy type I (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Senile cardiac amyloidosis	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Amyloid light-chain nephropathy (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
AA amyloid nephropathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	2
Hereditary cerebral amyloid angiopathy, Icelandic type	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Familial amyloid polyneuropathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Familial amyloid polyneuropathy, Iowa type	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Hepatic amyloidosis	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Familiær amyloid neuropati, finsk type	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type VI	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
familliær amyloid polyneuropati, type V	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Cerebral amyloid angiopathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Sporadic cerebral amyloid angiopathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Danish type familial amyloid cardiomyopathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Familial amyloid polyneuropathy, Jewish type	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Amyloidosis of spleen	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Cerebral amyloid angiopathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Sporadic cerebral amyloid angiopathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Hereditary cerebral amyloid angiopathy, Icelandic type	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Amyloid nephropathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Familial amyloid nephropathy with urticaria AND deafness	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Amyloid myopathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Gelatinous droplike corneal dystrophy (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Lattice corneal dystrophy (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Lattice corneal dystrophy Type I (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
dystrophia corneae latticis type 3	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
amyloidogen transthyretin amyloidose	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Cerebral amyloid angiopathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Sporadic cerebral amyloid angiopathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Amyloid pterygium	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	3
Hereditary cystatin C amyloid angiopathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Cerebral amyloid angiopathy associated with systemic amyloidosis	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	2
A rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Amyloidosis of small intestine (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare form of amyloidosis characterized by accumulation and extensive visceral deposition of an amyloidogenic variant of beta 2 microglobulin leading to progressive gastrointestinal dysfunction, Sjögren syndrome and autonomic neuropathy.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare, autosomal dominant neurological disorder due to truncation mutations of the prion protein gene PRNP (20p13) leading to deposition of prion protein amyloid. Onset is usually in the fourth decade of life and reported clinical manifestations include diarrhea, nausea, autonomic failure (areflexia, weakness), neurogenic bladder and urinary infections.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Hereditary amyloidosis (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare neurodegenerative disease with characteristics of progressive cognitive impairment, spastic tetraparesis and cerebellar ataxia resulting from amyloid deposits in the brain. Spasticity with increased deep tendon reflexes and tone are early symptoms, muscular rigidity evolves later. Progressive mental deterioration usually starts with apathy and impaired memory with progression to complete disorientation. Caused by heterozygous mutation in the ITM2B gene on chromosome 13q14.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare systemic amyloidosis with characteristics of a triad of ophthalmologic, neurologic and dermatologic findings due to the deposition of gelsolin amyloid fibrils in these tissues. Clinical manifestations include corneal lattice dystrophy, cranial neuropathy, especially affecting the facial nerve, bulbar signs, cutis laxa, increased skin fragility and less commonly peripheral neuropathy and renal failure. Caused by mutation in the gelsolin gene (GSN).	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	4
A rare neurodegenerative disease with characteristics of progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves. Caused by mutation in the ITM2B gene.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare systemic amyloidosis with characteristics of a triad of ophthalmologic, neurologic and dermatologic findings due to the deposition of gelsolin amyloid fibrils in these tissues. Clinical manifestations include corneal lattice dystrophy, cranial neuropathy, especially affecting the facial nerve, bulbar signs, cutis laxa, increased skin fragility and less commonly peripheral neuropathy and renal failure. Caused by mutation in the gelsolin gene (GSN).	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	3
familliær amyloid polyneuropati, type V	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Hemodialysis-associated amyloidosis	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	2
Hemodialysis-associated secondary amyloidosis of skin (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	3
Amyloid light-chain nephropathy (disorder)	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	6
Senile cardiac amyloidosis	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Senile brain amyloidosis	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	1
Primary systemic amyloidosis associated with occult plasma cell dyscrasia	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	4
Amyloid light chain amyloidosis due to multiple myeloma (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	4
AA amyloid nephropathy	Associated morphology	False	Amyloid deposition	Inferred relationship	Some	2
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Heredofamilial systemic amyloidosis affecting skin (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Secondary systemic amyloidosis affecting skin (AA fibril type) (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare neurodegenerative disease with characteristics of progressive cognitive impairment, spastic tetraparesis and cerebellar ataxia resulting from amyloid deposits in the brain. Spasticity with increased deep tendon reflexes and tone are early symptoms, muscular rigidity evolves later. Progressive mental deterioration usually starts with apathy and impaired memory with progression to complete disorientation. Caused by heterozygous mutation in the ITM2B gene on chromosome 13q14.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	4
Hereditary oculoleptomeningeal amyloid angiopathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Secondary systemic amyloidosis (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Amyloidosis of skin	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Systemic amyloidosis affecting skin (disorder)	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare nonhereditary systemic amyloidosis characterized by slowly progressive renal dysfunction, increased serum creatinine, mostly normal urine analysis with no significant proteinuria and associated heart disease. Cardiac involvement presents as hypertrophic obstructive cardiomyopathy, left ventricular outflow tract obstruction, coronary artery disease and conduction system abnormalities. Histology reveals medullar amyloid deposits, renal tubular atrophy, interstitial fibrosis, and glomerular sclerosis.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare, neurodegenerative disease characterized by progressive dementia and ataxia, widespread cerebral amyloid angiopathy and parenchymal amyloid deposition. Two subtypes have been identified, ABri amyloidosis and ADan amyloidosis.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare, neurodegenerative disease characterized by progressive dementia and ataxia, widespread cerebral amyloid angiopathy and parenchymal amyloid deposition. Two subtypes have been identified, ABri amyloidosis and ADan amyloidosis.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	2
A rare neurodegenerative disease with characteristics of progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves. Caused by mutation in the ITM2B gene.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	4
Cardiac familial non-neuropathic amyloidosis	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
Cerebral non-neuropathic heredofamilial amyloidosis angiopathy	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare, systemic amyloidosis characterized by slowly progressive renal disease presenting with proteinuria, hypertension and decreased glomerular filtration rate leading to progressive renal failure. Histology reveals amyloid deposits of leukocyte chemotactic factor-2 protein in the renal cortical interstitium, tubular basement membranes, glomeruli and the vessel walls. Extra-renal deposits can be seen in the liver, lungs, spleen and adrenal glands.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare, systemic amyloidosis characterized by the aggregation and deposition of amyloid fibrils composed of monoclonal immunoglobulin heavy-chain fragments, usually produced by a plasma cell neoplasm. Amyloid fibrils deposit in various organs, most commonly in the kidneys. It typically affects older patients and clinical presentation includes signs and symptoms of renal dysfunction, sometimes leading to nephrotic syndrome and end stage renal disease. Cardiac, liver and nerves involvement has also been described.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1
A rare genetic systemic disease characterised by adult onset, progressive sensorimotor and autonomic neuropathy and infiltrative cardiomyopathy. Neurological involvement usually starts with sensory loss in the extremities and progresses with motor neuropathy. Cardiomyopathy presents with rhythm abnormalities and heart failure. The disease also frequently manifests with a range of additional clinical signs and symptoms due to associated ocular, renal, central nervous system and gastrointestinal involvement.	Associated morphology	True	Amyloid deposition	Inferred relationship	Some	1

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Id	Description	Lang	Type	Status	Case?	Module
114258010	Amyloid deposition	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
114261011	Waxy deposition	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
114262016	Amyloid degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
114264015	Lardaceous degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
114265019	Amyloid	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
808663012	Amyloid deposition (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3072831000005112	amyloid aflejring	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)