4463009: Familial amyloid polyneuropathy, type II (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation générale à propos des tissus mous\Peripheral nerve finding\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\constatation générale à propos des tissus mous\Disorder of soft tissue\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II

\Disease\Genetic disease\maladie héréditaire\Hereditary amyloidosis (disorder)\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\affection dégénérative\Amyloidosis\Hereditary amyloidosis (disorder)\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\affection dégénérative\Amyloidosis\Systemic amyloidosis\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Neuropathy (disorder)\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\affection du système nerveux périphérique\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\affection du système nerveux périphérique\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\Familial disease\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\maladie systémique\Systemic amyloidosis\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type II
\Disease\Disorder of soft tissue\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\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	localisation d'une constatation (attribut)	nerf périphérique (structure corporelle)	true	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	est un(e) (attribut)	neuropathie amyloïde familiale	true	Inferred relationship	Some
Familial amyloid polyneuropathy, type II	morphologie associée (attribut)	Amyloid deposition	true	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	localisation d'une constatation (attribut)	structure du système nerveux périphérique	false	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	localisation d'une constatation (attribut)	nerf périphérique (structure corporelle)	false	Inferred relationship	Some	2
Familial amyloid polyneuropathy, type II	localisation d'une constatation (attribut)	structure d'un nerf	false	Inferred relationship	Some
Familial amyloid polyneuropathy, type II	localisation d'une constatation (attribut)	structure du système nerveux périphérique	false	Inferred relationship	Some	1
Familial amyloid polyneuropathy, type II	morphologie associée (attribut)	Amyloid deposition	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
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
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
781781013	Familial amyloid polyneuropathy, type II (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core