4463009: Familial amyloid polyneuropathy, type II (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Peripheral nerve finding\Peripheral neuropathy\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \General finding of soft tissue\Disorder of soft tissue\Peripheral neuropathy\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\Neurological disorder\Neuropathy\Peripheral neuropathy\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Peripheral neuropathy\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II
• \Disease\Disorder of body system\Neurological disorder\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 neuropathy\Polyneuropathy\Familial amyloid polyneuropathy\Familial amyloid polyneuropathy, type II

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start