SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital porphyria  190913009

Erythropoietic protoporphyria  51022005

Erythropoietic protoporphyria due to ferrochelatase deficiency   860859009

SNOMED CT code


SNOMED code860859009
nameErythropoietic protoporphyria due to ferrochelatase deficiency
statusactive
date introduced2020-07-31
fully specified name(s)Erythropoietic protoporphyria due to ferrochelatase deficiency (disorder)
synonymsErythropoietic protoporphyria due to ferrochelatase deficiency
attributes - group1
Due toFerrochelatase deficiency   276265003
attributes - group2
OccurrenceCongenital   255399007
parentsErythropoietic protoporphyria   51022005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital porphyria   190913009
          Erythropoietic protoporphyria   51022005
            Erythropoietic protoporphyria due to ferrochelatase deficiency   860859009

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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