Adrenoleukodystrophy   65389002

SNOMED CT code


SNOMED code65389002
nameAdrenoleukodystrophy
statusactive
date introduced2002-01-31
fully specified name(s)Adrenoleukodystrophy (disorder)
synonyms
  • Adrenoleukodystrophy
  • Bronze Schilder disease
  • Schilder-Addison complex
  • Siemerling-Creutzfeldt disease
  • X-linked adrenoleucodystrophy
  • Adrenoleucodystrophy
  • ALD - adrenoleukodystrophy
  • X-linked adrenoleukodystrophy
attributes - group4
OccurrenceCongenital   255399007
attributes - group3
Finding siteAdrenal cortex structure   68594002
attributes - group1
Finding siteMyelinated nerve fiber structure   54115001
Associated morphologyMyelin sheath alteration   125495003
attributes - group2
Finding siteWhite matter structure of brain and spinal cord   389080008
Associated morphologyDystrophy   4720007
parents
  • 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
children
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disease of the central nervous system   80690008
          Hereditary degenerative disease of central nervous system   106018006
            Adrenoleukodystrophy   65389002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Inherited metabolic disorder of nervous system   128190004
            Adrenoleukodystrophy   65389002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              Adrenoleukodystrophy   65389002

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

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Disorder of peroxisomal function   238059005
            Loss of single peroxisomal function   238066006
              Adrenoleukodystrophy   65389002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Hereditary disorder of endocrine system   363104002
            Adrenoleukodystrophy   65389002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Disorder of adrenal gland   30171000
          Disorder of adrenal cortex   129636003
            Adrenal cortical hypofunction   386584007
              Adrenoleukodystrophy   65389002

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.