SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Inborn error of metabolism  86095007

Trypsinogen deficiency   190953007

SNOMED CT code


SNOMED code190953007
nameTrypsinogen deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Trypsinogen deficiency (disorder)
synonymsTrypsinogen deficiency
attributes - group1
OccurrenceCongenital   255399007
parentsInborn error of metabolism   86095007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Trypsinogen deficiency   190953007

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

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