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1187126002: Integral membrane protein 2B related amyloidosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4670012017 Integral membrane protein 2B related amyloidosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4670013010 ITM2B-related cerebral amyloid angiopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4670014016 Integral membrane protein 2B related amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4670015015 ITM2B-related amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4670016019 ITM2B amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399570011 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399571010 A rare, neurodegenerative disease characterised by progressive dementia and ataxia, widespread cerebral amyloid angiopathy and parenchymal amyloid deposition. Two subtypes have been identified, ABri amyloidosis and ADan amyloidosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4670012017 Integral membrane protein 2B related amyloidosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4670013010 ITM2B-related cerebral amyloid angiopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4670014016 Integral membrane protein 2B related amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4670015015 ITM2B-related amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4670016019 ITM2B amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4670019014 A rare neurodegenerative disease with characteristics of progressive dementia and ataxia, widespread cerebral amyloid angiopathy and parenchymal amyloid deposition. Two subtypes have been identified, ABri amyloidosis and ADan amyloidosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399570011 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399571010 A rare, neurodegenerative disease characterised by progressive dementia and ataxia, widespread cerebral amyloid angiopathy and parenchymal amyloid deposition. Two subtypes have been identified, ABri amyloidosis and ADan amyloidosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3413851001000110 ITM2B-Amyloidose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6378421000241110 angiopathie amyloïde cérébrale familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6378431000241112 amylose associée à ITM2B (integral membrane protein 2B) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6378441000241119 angiopathie amyloïde cérébrale liée à ITM2B (integral membrane protein 2B) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6378421000241110 angiopathie amyloïde cérébrale familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6378431000241112 amylose associée à ITM2B (integral membrane protein 2B) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6378441000241119 angiopathie amyloïde cérébrale liée à ITM2B (integral membrane protein 2B) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3413851001000110 ITM2B-Amyloidose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Integral membrane protein 2B related amyloidosis (disorder) Is a Hereditary degenerative disease of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Chronic disease of cardiovascular system true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Cerebral amyloid angiopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Intracerebral vascular finding true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Vascular degeneration false Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Hereditary amyloidosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Chronic organic mental disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Dementia true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Degenerative brain disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 4
Integral membrane protein 2B related amyloidosis (disorder) Interprets Cognitive functions true Inferred relationship Existential restriction modifier (core metadata concept) 3
Integral membrane protein 2B related amyloidosis (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Integral membrane protein 2B related amyloidosis (disorder) Finding site Vascular structure within brain (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Integral membrane protein 2B related amyloidosis (disorder) Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier (core metadata concept) 1
Integral membrane protein 2B related amyloidosis (disorder) Finding site Structure of parenchyma of brain true Inferred relationship Existential restriction modifier (core metadata concept) 2
Integral membrane protein 2B related amyloidosis (disorder) Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier (core metadata concept) 2
Integral membrane protein 2B related amyloidosis (disorder) Is a Disorder of blood vessel (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Integral membrane protein 2B related amyloidosis (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial dementia British type (disorder) Is a True Integral membrane protein 2B related amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Is a True Integral membrane protein 2B related amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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