SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Heterozygous hemoglobinopathy  123773003

Hemoglobin C trait   76050008

SNOMED CT code


SNOMED code76050008
nameHemoglobin C trait
statusactive
date introduced2002-01-31
fully specified name(s)Hemoglobin C trait (disorder)
synonyms
  • Hemoglobin C trait
  • Hemoglobin C-A disorder
  • Heterozygous for Hb C
  • Haemoglobin C trait
  • Haemoglobin C-A disorder
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
  • Heterozygous hemoglobinopathy   123773003
  • Hereditary hemoglobinopathy due to globin chain mutation   127038008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Heterozygous hemoglobinopathy   123773003
            Hemoglobin C trait   76050008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Hereditary hemoglobinopathy due to globin chain mutation   127038008
            Hemoglobin C trait   76050008

ancestors
sorted most to least specific
cpt crosswalks

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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