Juvenile neuronal ceroid lipofuscinosis 61663001

SNOMED CT code

SNOMED code

61663001

name

Juvenile neuronal ceroid lipofuscinosis

status

active

date introduced

2002-01-31

fully specified name(s)

Juvenile neuronal ceroid lipofuscinosis (disorder)

synonyms

Juvenile neuronal ceroid lipofuscinosis
Batten-Mayou disease
Spielmeyer-Vogt disease
Amaurotic idiocy, juvenile type
Cerebral lipidosis, myoclonic variant
Batten-Spielmeyer-Vogt disease
Cerebral lipidosis myoclonic variant
Batten-Mayou syndrome
Amaurotic idiocy juvenile type
Spielmeyer-Vogt type neuronal ceroid lipofuscinosis

attributes - group2

Interprets

Movement 255324009

attributes - group4

Finding site

Brain structure 12738006

attributes - group3

Occurrence

Congenital 255399007

attributes - group1

Associated morphology

Lipochrome pigmentation 54436007

parents

Myoclonic disorder 127324008
Cerebral lipidosis 16517004
Disorder of pigmentation 414032001
Neuronal ceroid lipofuscinosis 42012007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of movement 298325004
Movement disorder 60342002
Myoclonic disorder 127324008
Juvenile neuronal ceroid lipofuscinosis 61663001

SNOMED CT Concept 138875005
Clinical finding 404684003
Central nervous system finding 246556002
Finding of brain 299718000
Disorder of brain 81308009
Cerebral lipidosis 16517004
Juvenile neuronal ceroid lipofuscinosis 61663001

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of pigmentation 414032001
Juvenile neuronal ceroid lipofuscinosis 61663001

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Degenerative disorder 362975008
Neuronal ceroid lipofuscinosis 42012007
Juvenile neuronal ceroid lipofuscinosis 61663001

ancestors

sorted most to least specific

Myoclonic disorder 127324008
Cerebral lipidosis 16517004
Disorder of pigmentation 414032001
Neuronal ceroid lipofuscinosis 42012007
Lipid storage disease 10741005
Inherited metabolic disorder of nervous system 128190004
Movement disorder 60342002
Disorder of brain 81308009
Lipofuscinosis 14210003
Lysosomal storage disease 28821000119102
Degenerative disorder 362975008
Disorder of lysosomal enzyme 23585005
Hereditary disorder of nervous system 363235000
Finding of movement 298325004
Disorder of head 118934005
Disorder of lipid storage and metabolism 238017009
Storage disease 34420000
Disorder of the central nervous system 23853001
Finding of brain 299718000
Disorder of nervous system 118940003
Head finding 406122000
Disorder of lipoprotein AND/OR lipid metabolism 48286001
Enzymopathy 78548001
Inborn error of metabolism 86095007
Hereditary disorder by system 363137000
Central nervous system finding 246556002
Disorder of body system 362965005
Congenital disease 66091009
Finding of head and neck region 118254002
Hereditary metabolic disease 1821000146108
Metabolic disease 75934005
Hereditary disease 32895009
Genetic disease 782964007
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Finding of movement 298325004

Movement disorder 60342002

Myoclonic disorder 127324008

Juvenile neuronal ceroid lipofuscinosis 61663001

SNOMED CT code