73663008: Neurologic xeroderma pigmentosum (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Neurologic xeroderma pigmentosum (disorder)
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Neurologic xeroderma pigmentosum (disorder)
• \Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Neurologic xeroderma pigmentosum (disorder)

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
122320010	Neurologic xeroderma pigmentosum	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
814076017	Neurologic xeroderma pigmentosum (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2548038016	Disorder of central nervous system due to xeroderma pigmentosum	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2113461000052114	sjukdom i centrala nervsystemet orsakad av xeroderma pigmentosum	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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