42295001: Familial amyloid polyneuropathy (disorder)

SNOMED CT Concept\Clinical finding\...

\General finding of soft tissue\Peripheral nerve finding\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy
\General finding of soft tissue\Disorder of soft tissue\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy

\Disease\Genetic disease\Hereditary disease\Hereditary amyloidosis\Familial amyloid polyneuropathy
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial amyloid polyneuropathy
\Disease\Degenerative disorder\Amyloidosis\Hereditary amyloidosis\Familial amyloid polyneuropathy
\Disease\Degenerative disorder\Amyloidosis\Systemic amyloidosis\Familial amyloid polyneuropathy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy
\Disease\Disorder of body system\Disorder of nervous system\Neuropathy\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the peripheral nervous system\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Familial amyloid polyneuropathy
\Disease\Familial disease\Familial amyloid polyneuropathy
\Disease\Systemic disease\Systemic amyloidosis\Familial amyloid polyneuropathy
\Disease\Disorder of soft tissue\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

70562011 Familial amyloid polyneuropathy en Synonym Active Entire term case insensitive SNOMED CT core module

70564012 AF type amyloidosis en Synonym Active Entire term case sensitive SNOMED CT core module

70566014 Familial polyneuropathic amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module

493270014 Familial neuropathic amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module

779178017 Familial amyloid polyneuropathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3035568014 Neuropathic heredofamilial amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial amyloid polyneuropathy	Is a	Hereditary peripheral neuropathy	true	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Is a	Polyneuropathy	true	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Is a	Familial disease	true	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Is a	Localized amyloidosis	false	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier	1
Familial amyloid polyneuropathy	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier	1
Familial amyloid polyneuropathy	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Is a	Amyloidosis	false	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Is a	Neurological lesion	false	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Associated morphology	Amyloid deposition	true	Inferred relationship	Existential restriction modifier	1
Familial amyloid polyneuropathy	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier	1
Familial amyloid polyneuropathy	Finding site	Peripheral nerve structure	false	Inferred relationship	Existential restriction modifier	2
Familial amyloid polyneuropathy	Is a	Degenerative disorder	false	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Is a	Hereditary amyloidosis	true	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Is a	Systemic amyloidosis	true	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy	Finding site	Peripheral nerve structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Amyloid polyneuropathy type I	Is a	False	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Familial amyloid neuropathy, Finnish type	Is a	False	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Amyloidosis, type I	Is a	False	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy, Jewish type	Is a	False	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy, type II	Is a	True	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy, type VI	Is a	True	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy, Iowa type	Is a	True	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Amyloid polyneuropathy type I	Is a	True	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy with cutaneous amyloidosis	Is a	True	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Familial amyloid polyneuropathy, Jewish type	Is a	True	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier
Disorder of glomerulus due to familial amyloid polyneuropathy	Due to	True	Familial amyloid polyneuropathy	Inferred relationship	Existential restriction modifier	2

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
70562011	Familial amyloid polyneuropathy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
70564012	AF type amyloidosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
70566014	Familial polyneuropathic amyloidosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
493270014	Familial neuropathic amyloidosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
779178017	Familial amyloid polyneuropathy (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3035568014	Neuropathic heredofamilial amyloidosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module