702421006: Familial encephalopathy with neuroserpin inclusion bodies (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain\Familial encephalopathy with neuroserpin inclusion bodies
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Familial encephalopathy with neuroserpin inclusion bodies

\Central nervous system finding\Finding of brain\Disorder of brain\Familial encephalopathy with neuroserpin inclusion bodies
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Familial encephalopathy with neuroserpin inclusion bodies

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Familial encephalopathy with neuroserpin inclusion bodies
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial encephalopathy with neuroserpin inclusion bodies
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Familial encephalopathy with neuroserpin inclusion bodies
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Familial encephalopathy with neuroserpin inclusion bodies
\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Familial encephalopathy with neuroserpin inclusion bodies
\Disease\Disorder of head (disorder)\Disorder of brain\Familial encephalopathy with neuroserpin inclusion bodies

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial encephalopathy with neuroserpin inclusion bodies	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial encephalopathy with neuroserpin inclusion bodies	Is a	Disorder of brain	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial encephalopathy with neuroserpin inclusion bodies	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial encephalopathy with neuroserpin inclusion bodies	Finding site	Brain 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
3009273013	Familial encephalopathy with neuroserpin inclusion bodies	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3009514013	Familial encephalopathy with neuroserpin inclusion bodies (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3009601017	Familial dementia with neuroserpin inclusion bodies	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3009273013	Familial encephalopathy with neuroserpin inclusion bodies	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3009273013	Familial encephalopathy with neuroserpin inclusion bodies	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3009514013	Familial encephalopathy with neuroserpin inclusion bodies (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3009514013	Familial encephalopathy with neuroserpin inclusion bodies (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3009601017	Familial dementia with neuroserpin inclusion bodies	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3009601017	Familial dementia with neuroserpin inclusion bodies	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3432891001000115	Enzephalopathie mit Neuroserpin-Einschlüssen, familiäre Form	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
923311000172117	encéphalopathie familiale avec corps d'inclusion de neuroserpine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
964711000172112	FENIB - familial encephalopathy with neuroserpin inclusion bodies	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
923311000172117	encéphalopathie familiale avec corps d'inclusion de neuroserpine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
964711000172112	FENIB - familial encephalopathy with neuroserpin inclusion bodies	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3432891001000115	Enzephalopathie mit Neuroserpin-Einschlüssen, familiäre Form	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module