4463009: Familial amyloid polyneuropathy, type II (disorder)

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

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

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

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
Familial amyloid polyneuropathy, type II	Is a	Familial amyloid polyneuropathy (disorder)	true	Inferred relationship	Some
Familial amyloid polyneuropathy, type II	Finding site	Nerve structure	false	Inferred relationship	Some
Familial amyloid polyneuropathy, type II	Finding site	Peripheral nervous system structure	false	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	Associated morphology	Amyloid deposition	false	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	Associated morphology	Amyloid deposition	true	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	Finding site	Peripheral nervous system structure	false	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	Finding site	Peripheral nerve structure	false	Inferred relationship	Some	2
Familial amyloid polyneuropathy, type II	Finding site	Peripheral nerve structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
7578013	Familial amyloid polyneuropathy, type II	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
7579017	Familial amyloid polyneuropathy, 84 Ser-for-Ile	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
7580019	Familial amyloid polyneuropathy, Indiana-Swiss type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
7581015	Amyloidosis, Indiana-Maryland type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
7582010	Hereditary neuropathic amyloidosis, type II	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
493960015	Indiana-Maryland type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
493961016	Familial amyloid polyneuropathy type II	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
493962011	German type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
493963018	Swiss type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
493964012	Rakavina type amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
781781013	Familial amyloid polyneuropathy, type II (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core