42295001: Familial amyloid polyneuropathy (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\General finding of soft tissue\Peripheral nerve finding\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)
\General finding of soft tissue\Disorder of soft tissue\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary amyloidosis (disorder)\Familial amyloid polyneuropathy (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial amyloid polyneuropathy (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the peripheral nervous system (disorder)\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the peripheral nervous system (disorder)\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy (disorder)
\Disease\Familial disease\Familial amyloid polyneuropathy (disorder)
\Disease\Systemic disease\Systemic amyloidosis\Familial amyloid polyneuropathy (disorder)
\Disease\Disorder of soft tissue\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)
\Disease\Amyloidosis\Hereditary amyloidosis (disorder)\Familial amyloid polyneuropathy (disorder)
\Disease\Amyloidosis\Systemic amyloidosis\Familial amyloid polyneuropathy (disorder)

Status: current, 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
Familial amyloid polyneuropathy (disorder)	Is a	Hereditary peripheral neuropathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Is a	Polyneuropathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Is a	Familial disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Is a	Localized amyloidosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid polyneuropathy (disorder)	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid polyneuropathy (disorder)	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Is a	Amyloidosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Is a	Neurological lesion	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Associated morphology	Amyloid deposition	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid polyneuropathy (disorder)	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid polyneuropathy (disorder)	Finding site	Peripheral nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial amyloid polyneuropathy (disorder)	Is a	Degenerative disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Is a	Hereditary amyloidosis (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Is a	Systemic amyloidosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy (disorder)	Finding site	Peripheral nerve structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Amyloid polyneuropathy type I	Is a	False	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid neuropathy, Finnish type	Is a	False	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Amyloidosis, type I	Is a	False	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, Jewish type	Is a	False	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, type II	Is a	True	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, type VI	Is a	True	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, Iowa type	Is a	True	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Amyloid polyneuropathy type I (disorder)	Is a	True	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder)	Is a	True	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, Jewish type	Is a	True	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disorder due to neuropathic heredofamilial amyloidosis	Due to	True	Familial amyloid polyneuropathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	2

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
70562011	Familial amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
70564012	AF type amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
70566014	Familial polyneuropathic amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
493270014	Familial neuropathic amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
779178017	Familial amyloid polyneuropathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3035568014	Neuropathic heredofamilial amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
70562011	Familial amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
70562011	Familial amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
70564012	AF type amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
70565013	Hereditary amyloidosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
70566014	Familial polyneuropathic amyloidosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
70566014	Familial polyneuropathic amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
493270014	Familial neuropathic amyloidosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
493270014	Familial neuropathic amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
779178017	Familial amyloid polyneuropathy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
779178017	Familial amyloid polyneuropathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3035568014	Neuropathic heredofamilial amyloidosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3035568014	Neuropathic heredofamilial amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3393761001000114	ATTRV30M-Amyloidose	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
100421000077110	neuropathie amyloïde familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
100421000077110	neuropathie amyloïde familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3393761001000114	ATTRV30M-Amyloidose	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module