SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Inborn error of metabolism  86095007

Disorder of peroxisomal function  238059005

General loss of peroxisomal function   238060000

SNOMED CT code


SNOMED code238060000
nameGeneral loss of peroxisomal function
statusactive
date introduced2002-01-31
fully specified name(s)General loss of peroxisomal function (disorder)
synonymsGeneral loss of peroxisomal function
attributes - group1
OccurrenceCongenital   255399007
parentsDisorder of peroxisomal function   238059005
childrenAlpha-methylacyl-CoA racemase deficiency disorder   700463002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Disorder of peroxisomal function   238059005
            General loss of peroxisomal function   238060000

ancestors
sorted most to least specific
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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.

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