5134006: Familial amyloid polyneuropathy, type VI (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 VI (disorder)
• \constatation générale à propos des tissus mous\Disorder of soft tissue\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary amyloidosis (disorder)\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)
• \Disease\affection dégénérative\Amyloidosis\Hereditary amyloidosis (disorder)\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)
• \Disease\affection dégénérative\Amyloidosis\Systemic amyloidosis\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)
• \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 VI (disorder)
• \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 VI (disorder)
• \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 VI (disorder)
• \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 VI (disorder)
• \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 VI (disorder)
• \Disease\Familial disease\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)
• \Disease\maladie systémique\Systemic amyloidosis\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)
• \Disease\Disorder of soft tissue\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, type VI (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
789229012	Familial amyloid polyneuropathy, type VI (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
9598011	Familial amyloid polyneuropathy, type VI	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
9599015	Familial amyloid polyneuropathy, 60 Ala-for-Thr	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
9600017	Familial amyloid polyneuropathy, Appalachian type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

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

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