Congenital porphyria   190913009

SNOMED CT code


SNOMED code190913009
nameCongenital porphyria
statusactive
date introduced2002-01-31
fully specified name(s)Congenital porphyria (disorder)
synonymsCongenital porphyria
attributes - group1
OccurrenceCongenital   255399007
parents
children
  • Congenital erythropoietic porphyria   22935002
  • Erythropoietic protoporphyria   51022005
  • Porphobilinogen synthase deficiency   64081000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of porphyrin metabolism   29094004
          Inherited disorder of porphyrin metabolism   403832004
            Congenital porphyria   190913009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of porphyrin metabolism   29094004
          Porphyria   418470004
            Congenital porphyria   190913009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital porphyria   190913009

ancestors
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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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