718849008: X-linked neurodegenerative syndrome Bertini type (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding related to coordination / incoordination\Ataxia\Hereditary ataxia\X-linked neurodegenerative syndrome Bertini type
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\X-linked neurodegenerative syndrome Bertini type
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\X-linked neurodegenerative syndrome Bertini type
• \Disease\Degenerative disorder\X-linked neurodegenerative syndrome Bertini type
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\X-linked neurodegenerative syndrome Bertini type
• \Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary ataxia\X-linked neurodegenerative syndrome Bertini type
• \Disease\Congenital disease\X-linked neurodegenerative syndrome Bertini type

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3314126017	X-linked neurodegenerative syndrome Bertini type (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3314127014	X-linked neurodegenerative syndrome Bertini type	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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