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 II   767498008

SNOMED CT code


SNOMED code767498008
nameAutosomal recessive congenital methemoglobinemia type II
statusactive
date introduced2018-07-31
fully specified name(s)Autosomal recessive congenital methemoglobinemia type II (disorder)
synonyms
  • Autosomal recessive congenital methaemoglobinaemia type II
  • Autosomal recessive congenital methemoglobinemia type II
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 II   767498008

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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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