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 (disorder)\Hereditary disorder of nervous system (disorder)\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\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the peripheral nervous system (disorder)\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the peripheral nervous system (disorder)\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
• \Disease\Amyloidosis\Hereditary amyloidosis (disorder)\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, type II
• \Disease\Amyloidosis\Systemic amyloidosis\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:

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
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

Expanded Value Set

This concept is not in any reference sets

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