SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Heterozygous hemoglobinopathy  123773003

Hemoglobin O-Arab trait   445542007

SNOMED CT code


SNOMED code445542007
nameHemoglobin O-Arab trait
statusactive
date introduced2010-07-31
fully specified name(s)Hemoglobin O-Arab trait (disorder)
synonyms
  • Hemoglobin O-Arab trait
  • Haemoglobin O-Arab trait
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 O-Arab trait   445542007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Hereditary hemoglobinopathy due to globin chain mutation   127038008
            Hemoglobin O-Arab trait   445542007

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:
  • CPT® to SNOMED Crosswalks

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