Westphal-Strumpell syndrome 190823004

SNOMED CT code

SNOMED code

190823004

name

Westphal-Strumpell syndrome

status

active

date introduced

2002-01-31

fully specified name(s)

Westphal-Strumpell syndrome (disorder)

synonyms

Westphal-Strumpell syndrome
Westphal-Strumpell cerebral pseudosclerosis
Pseudosclerotic type of Wilson's disease
Westphal-Strumpell form of Wilson's disease

attributes - group1

Associated morphology

Degenerative abnormality 107669003

Finding site

Liver structure 10200004

attributes - group2

Associated morphology

Degenerative abnormality 107669003

Finding site

Brain structure 12738006

attributes - group3

Associated morphology

Degenerative abnormality 107669003

Finding site

Body tissue structure 85756007

attributes - group4

Interprets

Movement 255324009

attributes - group5

Finding site

Basal ganglion structure 32610002

attributes - group6

Interprets

Movement observable 363847004

Has interpretation

Abnormal 263654008

parents

Wilson's disease 88518009

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of movement 298325004
Involuntary movement 267078001
Chorea 271700006
Wilson's disease 88518009
Westphal-Strumpell syndrome 190823004

ancestors

sorted most to least specific

Wilson's disease 88518009
Hereditary degenerative disease of central nervous system 106018006
Metabolic and genetic disorder affecting the liver 235903001
Chorea 271700006
Digestive system hereditary disorder 363080007
Degenerative brain disorder 52522001
Disorder of copper metabolism 79886009
Autosomal recessive hereditary disorder 85995004
Hereditary disorder of nervous system 363235000
Disease of liver 235856003
Involuntary movement 267078001
Degenerative disease of the central nervous system 80690008
Disorder of mineral metabolism 45744005
Autosomal hereditary disorder 1899006
Disorder of basal ganglia 70835005
Extrapyramidal disease 76349003
Disorder of liver and/or biliary tract 1290917001
Hereditary disorder by system 363137000
Metabolic disease 75934005
Liver finding 249565005
Finding of head region 298364001
Movement disorder 60342002
Disorder of brain 81308009
Degenerative disorder 362975008
Disorder of abdomen 118948005
Finding of movement 298325004
Hereditary disease 32895009
Disorder of the central nervous system 23853001
Abdominal organ finding 249561001
Disorder of digestive organ 76712006
Disorder of head 118934005
Finding of brain 299718000
Disorder of nervous system 118940003
Finding of abdomen 609624008
Genetic disease 782964007
Viscus structure finding 406123005
Disorder of digestive system 53619000
Disorder of abdominopelvic segment of trunk 822988000
Head finding 406122000
Central nervous system finding 246556002
Disorder of body system 362965005
Finding of abdominopelvic segment of trunk 822987005
Disorder of trunk 128121009
Finding of head and neck region 118254002
Digestive system finding 386617003
Disease 64572001
Finding of trunk structure 302292003
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Finding of movement 298325004

Involuntary movement 267078001

Chorea 271700006

Wilson's disease 88518009

Westphal-Strumpell syndrome 190823004

SNOMED CT code