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68790008: Amyloid deposition (morphologic abnormality)

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

Descriptions:

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
114258010 Amyloid deposition en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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
114263014 Hyaloid degeneration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
114264015 Lardaceous degeneration en Synonym (core metadata concept) Active Only initial character 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 Only initial character 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 Only initial character 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

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyloid deposition Is a Deposition true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial localized cutaneous amyloidosis (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept)
Secondary localized cutaneous amyloidosis Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept)
Systemic amyloidosis affecting skin (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept)
Amyloidosis limited to skin (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyloidosis of spleen Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular amyloid deposit Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Type I Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Type II Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Type II Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
syndrome de Meretoja Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Type III Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Gelatinous droplike corneal dystrophy Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Type II Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Type II Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Type II Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Type II Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 3
Amyloid light-chain nephropathy (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial visceral amyloidosis, Ostertag type Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloid A nephropathy (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid nephropathy with urticaria AND deafness Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloid nephropathy Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial visceral amyloidosis, Ostertag type Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloid disease of the urethra (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated atrial amyloid Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary familial amyloid myopathy (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular amyloid deposit Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Conjunctival amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary sporadic amyloid myopathy Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloid polyneuropathy type I (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Senile cardiac amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloid light-chain nephropathy (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloid A nephropathy (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid polyneuropathy (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid polyneuropathy, Iowa type Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Hepatic amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid neuropathy, Finnish type Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid polyneuropathy, type VI Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid polyneuropathy, type II Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
syndrome de Meretoja Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Cerebral amyloid angiopathy Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic cerebral amyloid angiopathy (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Danish type familial amyloid cardiomyopathy Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid polyneuropathy, Jewish type Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloidosis of spleen Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Cerebral amyloid angiopathy Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Sporadic cerebral amyloid angiopathy (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyloid nephropathy Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial amyloid nephropathy with urticaria AND deafness Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloid myopathy Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Gelatinous droplike corneal dystrophy Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Type I Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Type III Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyloidogenic transthyretin amyloidosis Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Cerebral amyloid angiopathy Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic cerebral amyloid angiopathy (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloid pterygium Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary cystatin C amyloid angiopathy Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Cerebral amyloid angiopathy associated with systemic amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Transthyretin related familial amyloid cardiomyopathy (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloidosis of small intestine Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant beta2-microglobulinic amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 1
Hereditary amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial dementia British type (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
AGel amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 4
ADan amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
AGel amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 3
syndrome de Meretoja Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Hemodialysis-associated amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Hemodialysis-associated secondary amyloidosis of skin (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 3
Amyloid light-chain nephropathy (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 6
Senile cardiac amyloidosis Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Senile brain amyloidosis (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary systemic amyloidosis associated with occult plasma cell dyscrasia Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 4
Amyloid light chain amyloidosis due to multiple myeloma (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 4
Amyloid A nephropathy (disorder) Associated morphology False Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Heredofamilial systemic amyloidosis affecting skin (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary systemic amyloidosis affecting skin (AA fibril type) (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial dementia British type (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary oculoleptomeningeal amyloid angiopathy (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary systemic amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyloidosis of skin Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Systemic amyloidosis affecting skin (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Apolipoprotein A-IV amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Integral membrane protein 2B related amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Integral membrane protein 2B related amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 2
ADan amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 4
Familial non-neuropathic amyloidosis of heart (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Cerebral non-neuropathic heredofamilial amyloidosis angiopathy Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
ALECT2 amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
AH amyloidosis (disorder) Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary ATTR amyloidosis Associated morphology True Amyloid deposition Inferred relationship Existential restriction modifier (core metadata concept) 1

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