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

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

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

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 (core metadata concept)	SNOMED CT core
3314127014	X-linked neurodegenerative syndrome Bertini type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401883016	An X-linked syndromic intellectual disability characterized by congenital ataxia and generalized hypotonia, global developmental delay with intellectual disability, myoclonic encephalopathy, progressive neurological deterioration, macular degeneration, and recurrent bronchopulmonary infections.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401884010	An X-linked syndromic intellectual disability characterised by congenital ataxia and generalised hypotonia, global developmental delay with intellectual disability, myoclonic encephalopathy, progressive neurological deterioration, macular degeneration, and recurrent bronchopulmonary infections.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3314126017	X-linked neurodegenerative syndrome Bertini type (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3314127014	X-linked neurodegenerative syndrome Bertini type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3314128016	This syndrome is characterised by generalised hypotonia, psychomotor deficit, congenital ataxia and recurrent bronchopulmonary infections. It has been described in seven males from three generations of a family. Five of them died during the first years of life and the remaining patients developed myoclonic encephalopathy and macular degeneration. The locus has been mapped to Xp22.33-pter.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3314129012	This syndrome is characterized by generalized hypotonia, psychomotor deficit, congenital ataxia and recurrent bronchopulmonary infections. It has been described in seven males from three generations of a family. Five of them died during the first years of life and the remaining patients developed myoclonic encephalopathy and macular degeneration. The locus has been mapped to Xp22.33-pter.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401883016	An X-linked syndromic intellectual disability characterized by congenital ataxia and generalized hypotonia, global developmental delay with intellectual disability, myoclonic encephalopathy, progressive neurological deterioration, macular degeneration, and recurrent bronchopulmonary infections.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401884010	An X-linked syndromic intellectual disability characterised by congenital ataxia and generalised hypotonia, global developmental delay with intellectual disability, myoclonic encephalopathy, progressive neurological deterioration, macular degeneration, and recurrent bronchopulmonary infections.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3384751001000114	Neurodegeneratives Syndrom, X-chromosomales, Typ Bertini	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
908711000172119	syndrome neurodégénératif lié à l'X type Bertini	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
908711000172119	syndrome neurodégénératif lié à l'X type Bertini	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3384751001000114	Neurodegeneratives Syndrom, X-chromosomales, Typ Bertini	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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