41590007: Familial amyloid polyneuropathy, Jewish type (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, Jewish type
• \constatation générale à propos des tissus mous\Disorder of soft tissue\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \Disease\Genetic disease\maladie héréditaire\Hereditary amyloidosis (disorder)\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \Disease\affection dégénérative\Amyloidosis\Hereditary amyloidosis (disorder)\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \Disease\affection dégénérative\Amyloidosis\Systemic amyloidosis\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \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, Jewish type
• \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, Jewish type
• \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, Jewish type
• \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, Jewish type
• \Disease\Familial disease\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \Disease\maladie systémique\Systemic amyloidosis\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type
• \Disease\Disorder of soft tissue\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Familial amyloid polyneuropathy, Jewish type

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
2164018013	Jewish type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
69375018	Familial amyloid polyneuropathy, Jewish type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
69376017	Familial amyloid polyneuropathy, 33 Ile-for-Phe	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
778394014	Familial amyloid polyneuropathy, Jewish type (disorder)	en	Fully specified name	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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