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

PEX26 deficiency   1187522009

SNOMED CT code


SNOMED code1187522009
namePEX26 deficiency
statusactive
date introduced2022-01-31
fully specified name(s)Peroxisome biogenesis disorder due to PEX26 mutation (disorder)
synonyms
  • PEX26 deficiency
  • Peroxisome biogenesis disorder due to PEX26 mutation
attributes - group1
OccurrenceCongenital   255399007
parentsPeroxisome biogenesis disorder   742876007
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
            Peroxisome biogenesis disorder   742876007
              PEX26 deficiency   1187522009

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.