783161005: Familial dementia British type (disorder)

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

Inbound Relationships

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Active

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Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3757895010	Familial dementia British type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3757896011	Familial dementia British type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3757897019	ABri amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3896360018	Familial British dementia with amyloid angiopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3757898012	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.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2156961000172111	amylose ABri	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
2156971000172119	démence familiale : type britannique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
2156981000172116	ABri-amyloïdose	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)