398229007: Amyloid polyneuropathy type I (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\Amyloid polyneuropathy type I (disorder)
• \constatation générale à propos des tissus mous\Disorder of soft tissue\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary amyloidosis (disorder)\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\affection dégénérative\Amyloidosis\Hereditary amyloidosis (disorder)\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\affection dégénérative\Amyloidosis\Systemic amyloidosis\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Neuropathy (disorder)\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (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\Amyloid polyneuropathy type I (disorder)
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\affection du système nerveux périphérique\Hereditary peripheral neuropathy\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\Familial disease\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\maladie systémique\Systemic amyloidosis\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)
• \Disease\Disorder of soft tissue\atteinte d'un nerf périphérique\polyneuropathie\neuropathie amyloïde familiale\Amyloid polyneuropathy type I (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1766148016	Amyloid polyneuropathy type I (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1777779015	Amyloid polyneuropathy type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2477007017	Familial amyloid neuropathy, Andrade type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2477008010	Hereditary amyloid polyneuropathy Portuguese type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2477009019	Familial amyloid polyneuropathy, 30 Met-for-Val	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2477010012	Familial amyloid neuropathy, Portuguese type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2477011011	Hereditary neuropathic amyloidosis, type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2477012016	Portuguese polyneuritic amyloidosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2477013014	Swedish type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2477014015	Amyloidosis, type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2477015019	Andrade type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2477016018	Andrade syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2477017010	Corino de Andrade paramyloidosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2477018017	Wohlwill-Corino Andrade syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2477019013	Portuguese type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2477020019	Japanese type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

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

Description inactivation indicator reference set

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US English

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