SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital methemoglobinemia  267550008

Autosomal recessive congenital methemoglobinemia  767497003

Autosomal recessive congenital methemoglobinemia type I   767499000

SNOMED CT code


SNOMED code767499000
nameAutosomal recessive congenital methemoglobinemia type I
statusactive
date introduced2018-07-31
fully specified name(s)Autosomal recessive congenital methemoglobinemia type I (disorder)
synonyms
  • Autosomal recessive congenital methemoglobinemia type I
  • Autosomal recessive congenital methaemoglobinaemia type I
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parentsAutosomal recessive congenital methemoglobinemia   767497003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital methemoglobinemia   267550008
          Autosomal recessive congenital methemoglobinemia   767497003
            Autosomal recessive congenital methemoglobinemia type I   767499000

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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.

Access to this feature is available in the following products:
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