Neonatal adrenoleucodystrophy 238061001

SNOMED CT code

SNOMED code

238061001

name

Neonatal adrenoleucodystrophy

status

active

date introduced

2002-01-31

fully specified name(s)

Neonatal adrenoleukodystrophy (disorder)

synonyms

Neonatal adrenoleukodystrophy
Neonatal adrenoleucodystrophy

attributes - group2

Finding site

Myelinated nerve fiber structure 54115001

Associated morphology

Myelin sheath alteration 125495003

attributes - group3

Finding site

White matter structure of brain and spinal cord 389080008

Associated morphology

Dystrophy 4720007

attributes - group1

Occurrence

Congenital 255399007

Finding site

Adrenal cortex structure 68594002

parents

Adrenoleukodystrophy 65389002
Peroxisome biogenesis disorder 742876007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Neurological lesion 299735001
Leukodystrophy 192781003
Adrenoleukodystrophy 65389002
Neonatal adrenoleucodystrophy 238061001

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Inborn error of metabolism 86095007
Disorder of peroxisomal function 238059005
Peroxisome biogenesis disorder 742876007
Neonatal adrenoleucodystrophy 238061001

ancestors

sorted most to least specific

Adrenoleukodystrophy 65389002
Peroxisome biogenesis disorder 742876007
Hereditary degenerative disease of central nervous system 106018006
Inherited metabolic disorder of nervous system 128190004
X-linked hereditary disease 128430005
Leukodystrophy 192781003
Loss of single peroxisomal function 238066006
Hereditary disorder of endocrine system 363104002
Adrenal cortical hypofunction 386584007
Autosomal recessive hereditary disorder 85995004
Hereditary disorder of nervous system 363235000
Disorder of peroxisomal function 238059005
Sex-linked hereditary disorder 82852009
Neurological lesion 299735001
Disorder of adrenal cortex 129636003
Degenerative disease of the central nervous system 80690008
Autosomal hereditary disorder 1899006
Neuropathy 386033004
Hypoadrenalism 237785004
Inborn error of metabolism 86095007
Disorder of adrenal gland 30171000
Disorder of the central nervous system 23853001
Hereditary disorder by system 363137000
Degenerative disorder 362975008
Disorder of nervous system 118940003
Hereditary metabolic disease 1821000146108
Disorder of endocrine system 362969004
Abdominal organ finding 249561001
Congenital disease 66091009
Disorder of retroperitoneum 734045002
Central nervous system finding 246556002
Disorder of body system 362965005
Hereditary disease 32895009
Viscus structure finding 406123005
Metabolic disease 75934005
Disorder of abdomen 118948005
Genetic disease 782964007
Finding of abdomen 609624008
Disorder of abdominopelvic segment of trunk 822988000
Finding of abdominopelvic segment of trunk 822987005
Disorder of trunk 128121009
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

Neurological lesion 299735001

Leukodystrophy 192781003

Adrenoleukodystrophy 65389002

Neonatal adrenoleucodystrophy 238061001

SNOMED CT code