4463009: Familial amyloid polyneuropathy, type II (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Peripheral nerve finding\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \General finding of soft tissue\Disorder of soft tissue\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Genetic disease\Hereditary disease\Hereditary amyloidosis\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Degenerative disorder\Amyloidosis\Hereditary amyloidosis\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Degenerative disorder\Amyloidosis\Systemic amyloidosis\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Disorder of nervous system\Neuropathy\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Disorder of nervous system\Disorder of the peripheral nervous system\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Disorder of nervous system\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Familial disease\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Systemic disease\Systemic amyloidosis\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of soft tissue\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
7578013	Familial amyloid polyneuropathy, type II	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
7579017	Familial amyloid polyneuropathy, 84 Ser-for-Ile	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
7580019	Familial amyloid polyneuropathy, Indiana-Swiss type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
7581015	Amyloidosis, Indiana-Maryland type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
7582010	Hereditary neuropathic amyloidosis, type II	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
493960015	Indiana-Maryland type amyloid polyneuropathy	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
493961016	Familial amyloid polyneuropathy type II	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
493962011	German type amyloid polyneuropathy	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
493963018	Swiss type amyloid polyneuropathy	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
493964012	Rakavina type amyloidosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
781781013	Familial amyloid polyneuropathy, type II (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start