Globoid cell leukodystrophy, late-onset 41142009

SNOMED CT code

SNOMED code

41142009

name

Globoid cell leukodystrophy, late-onset

status

active

date introduced

2002-01-31

fully specified name(s)

Globoid cell leukodystrophy, late-onset (disorder)

synonyms

Adult type Krabbe disease
Late onset Krabbe disease
Globoid cell leucodystrophy late onset
Galactocerebroside beta-galactosidase deficiency - late onset
Globoid cell leucodystrophy, late-onset
Globoid cell leukodystrophy, late-onset
Adult-type globoid cell leukodystrophy
Adult-type Krabbe's disease

attributes - group1

Occurrence

Adulthood 41847000

Associated morphology

Myelin sheath alteration 125495003

Finding site

Myelinated nerve fiber structure 54115001

attributes - group2

Occurrence

Adulthood 41847000

Associated morphology

Dystrophy 4720007

Finding site

White matter structure of brain and spinal cord 389080008

attributes - group3

Occurrence

Congenital 255399007

parents

Galactosylceramide beta-galactosidase deficiency 192782005

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Neurological lesion 299735001
Leukodystrophy 192781003
Galactosylceramide beta-galactosidase deficiency 192782005
Globoid cell leukodystrophy, late-onset 41142009

ancestors

sorted most to least specific

Galactosylceramide beta-galactosidase deficiency 192782005
Hereditary degenerative disease of central nervous system 106018006
Inherited metabolic disorder of nervous system 128190004
Leukodystrophy 192781003
Sphingolipidosis 238028008
Autosomal recessive hereditary disorder 85995004
Hereditary disorder of nervous system 363235000
Neurological lesion 299735001
Disorder of lipid storage and metabolism 238017009
Autosomal hereditary disorder 1899006
Degenerative disease of the central nervous system 80690008
Neuropathy 386033004
Lysosomal storage disease 28821000119102
Disorder of lipoprotein AND/OR lipid metabolism 48286001
Disorder of the central nervous system 23853001
Hereditary disorder by system 363137000
Storage disease 34420000
Degenerative disorder 362975008
Enzymopathy 78548001
Disorder of nervous system 118940003
Inborn error of metabolism 86095007
Central nervous system finding 246556002
Disorder of body system 362965005
Hereditary metabolic disease 1821000146108
Congenital disease 66091009
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

Neurological lesion 299735001

Leukodystrophy 192781003

Galactosylceramide beta-galactosidase deficiency 192782005

Globoid cell leukodystrophy, late-onset 41142009

SNOMED CT code