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718174008: Infantile striatonigral degeneration (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3310403014 Infantile striatonigral degeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310404015 Infantile striatonigral degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311374010 Infantile bilateral striatal necrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401687018 Infantile bilateral striatal necrosis (IBSN) comprises several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401688011 Infantile bilateral striatal necrosis (IBSN) comprises several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterised by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3310403014 Infantile striatonigral degeneration (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3310403014 Infantile striatonigral degeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310404015 Infantile striatonigral degeneration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3310404015 Infantile striatonigral degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311374010 Infantile bilateral striatal necrosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311374010 Infantile bilateral striatal necrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311375011 Comprises of several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus with characteristics of developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. Can be familial or sporadic. The familial form has an insidious onset and a slowly progressive downhill course, while the sporadic form is associated with abrupt neurologic dysfunction following an acute systemic febrile illness such as a mycoplasma, measles or streptococcus infection. Familial disease can be inherited as an autosomal recessive or mitochondrial disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401687018 Infantile bilateral striatal necrosis (IBSN) comprises several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401688011 Infantile bilateral striatal necrosis (IBSN) comprises several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterised by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3426201001000114 Striatale Nekrose, infantile de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996221000241112 dégénérescence striatonigrique de l'enfant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996231000241114 nécrose striatale bilatérale de l'enfant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996221000241112 dégénérescence striatonigrique de l'enfant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5996231000241114 nécrose striatale bilatérale de l'enfant fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3426201001000114 Striatale Nekrose, infantile de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infantile striatonigral degeneration (disorder) Is a Striatonigral degeneration true Inferred relationship Existential restriction modifier (core metadata concept)
Infantile striatonigral degeneration (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile striatonigral degeneration (disorder) Occurrence Infancy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile striatonigral degeneration (disorder) Finding site Structure of nigrostriate fiber (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile striatonigral degeneration (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile striatonigral degeneration (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 3
Infantile striatonigral degeneration (disorder) Has interpretation Slow true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group
Sporadic infantile bilateral striatal necrosis Is a True Infantile striatonigral degeneration (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile bilateral striatal necrosis Is a True Infantile striatonigral degeneration (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

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

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