41590007: Familial amyloid polyneuropathy, Jewish type (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, Jewish type
\General finding of soft tissue\Disorder of soft tissue\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type

\Disease\Genetic disease\Hereditary disease\Hereditary amyloidosis (disorder)\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type
\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, Jewish type
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type
\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, Jewish type
\Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type
\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, Jewish type
\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, Jewish type
\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, Jewish type
\Disease\Familial disease\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type
\Disease\Systemic disease\Systemic amyloidosis\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type
\Disease\Disorder of soft tissue\Peripheral nerve disease\Polyneuropathy\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type
\Disease\Amyloidosis\Hereditary amyloidosis (disorder)\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type
\Disease\Amyloidosis\Systemic amyloidosis\Familial amyloid polyneuropathy (disorder)\Familial amyloid polyneuropathy, Jewish type

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial amyloid polyneuropathy, Jewish type	Is a	Familial amyloid polyneuropathy (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, Jewish type	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid polyneuropathy, Jewish type	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid polyneuropathy, Jewish type	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, Jewish type	Is a	Amyloid polyneuropathy type I (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, Jewish type	Is a	Familial amyloid polyneuropathy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial amyloid polyneuropathy, Jewish type	Associated morphology	Amyloid deposition	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid polyneuropathy, Jewish type	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial amyloid polyneuropathy, Jewish type	Finding site	Peripheral nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial amyloid polyneuropathy, Jewish type	Finding site	Peripheral nerve structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
69375018	Familial amyloid polyneuropathy, Jewish type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
69376017	Familial amyloid polyneuropathy, 33 Ile-for-Phe	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
778394014	Familial amyloid polyneuropathy, Jewish type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2164018013	Jewish type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
69375018	Familial amyloid polyneuropathy, Jewish type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
69376017	Familial amyloid polyneuropathy, 33 Ile-for-Phe	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
778394014	Familial amyloid polyneuropathy, Jewish type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2164018013	Jewish type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2164018013	Jewish type amyloid polyneuropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4525901000241110	polyneuropathie amyloïde familiale de type juif	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4525901000241110	polyneuropathie amyloïde familiale de type juif	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module