718174008: Infantile striatonigral degeneration (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of movement\Bradykinesia\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Finding of movement\Movement disorder\Extrapyramidal disease\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration

\Central nervous system finding\Finding of brain\Encephalopathy\Disorder of brain stem\Disorder of midbrain\Striatonigral degeneration\Infantile striatonigral degeneration
\Central nervous system finding\Finding of brain\Encephalopathy\Extrapyramidal disease\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Central nervous system finding\Finding of brain\Encephalopathy\Disorder of basal ganglia\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Central nervous system finding\Finding of brain\Encephalopathy\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration
\Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Disorder of brain stem\Disorder of midbrain\Striatonigral degeneration\Infantile striatonigral degeneration
\Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Extrapyramidal disease\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Disorder of basal ganglia\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration
\Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration

\Finding of head and neck region\Head finding\...

\Finding of brain\Encephalopathy\...

\Disorder of brain stem\Disorder of midbrain\Striatonigral degeneration\Infantile striatonigral degeneration

\Extrapyramidal disease\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration

\Disorder of basal ganglia\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration

\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration

\Finding of head region\Disorder of basal ganglia\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration

\Disorder of head\Encephalopathy\...

\Disorder of brain stem\Disorder of midbrain\Striatonigral degeneration\Infantile striatonigral degeneration

\Extrapyramidal disease\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration

\Disorder of basal ganglia\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration

\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration

\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Disorder of brain stem\Disorder of midbrain\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Extrapyramidal disease\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Disorder of basal ganglia\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of head\Encephalopathy\Disorder of brain stem\Disorder of midbrain\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of head\Encephalopathy\Extrapyramidal disease\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of head\Encephalopathy\Disorder of basal ganglia\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Disorder of head\Encephalopathy\Degenerative brain disorder\Cerebral degeneration\Striatonigral degeneration\Infantile striatonigral degeneration
\Disease\Movement disorder\Extrapyramidal disease\Parkinsonism\Striatonigral degeneration\Infantile striatonigral degeneration

Status: current, Primitive. 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 Case insensitive SNOMED CT core

3310404015 Infantile striatonigral degeneration en Synonym Active Case insensitive SNOMED CT core

3311374010 Infantile bilateral striatal necrosis en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Infantile striatonigral degeneration	Associated morphology	Degenerative abnormality	true	Inferred relationship	Some	1
Infantile striatonigral degeneration	Interprets	Movement	true	Inferred relationship	Some	3
Infantile striatonigral degeneration	Has interpretation	Slow	true	Inferred relationship	Some	3
Infantile striatonigral degeneration	Is a	Striatonigral degeneration	true	Inferred relationship	Some
Infantile striatonigral degeneration	Associated morphology	Degeneration	false	Inferred relationship	Some	1
Infantile striatonigral degeneration	Occurrence	Infancy	true	Inferred relationship	Some	1
Infantile striatonigral degeneration	Finding site	Nigrostriate fibres	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sporadic infantile bilateral striatal necrosis	Is a	True	Infantile striatonigral degeneration	Inferred relationship	Some
Familial infantile bilateral striatal necrosis	Is a	True	Infantile striatonigral degeneration	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3310403014	Infantile striatonigral degeneration (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3310404015	Infantile striatonigral degeneration	en	Synonym	Active	Case insensitive	SNOMED CT core
3311374010	Infantile bilateral striatal necrosis	en	Synonym	Active	Case insensitive	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	Case sensitive	SNOMED CT core