SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital deficiency of intrinsic factor   234361004

SNOMED CT code


SNOMED code234361004
nameCongenital deficiency of intrinsic factor
statusactive
date introduced2002-01-31
fully specified name(s)Congenital deficiency of intrinsic factor (disorder)
synonymsCongenital deficiency of intrinsic factor
attributes - group4
Due toCobalamin deficiency   190634004
attributes - group3
OccurrenceCongenital   255399007
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital deficiency of intrinsic factor   234361004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Nutritional deficiency associated condition   363246002
        Megaloblastic anemia due to vitamin B>12< deficiency   49472006
          Pernicious anemia   84027009
            Congenital deficiency of intrinsic factor   234361004

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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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