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 disease   51053007

SNOMED CT code


SNOMED code51053007
nameHemoglobin C disease
statusactive
date introduced2002-01-31
fully specified name(s)Hemoglobin C disease (disorder)
synonyms
  • Homozygous for Hb C
  • Haemoglobin C disease
  • Haemoglobin C-C disease
  • Hemoglobin C disease
  • Hemoglobin C-C disease
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parentsHereditary hemoglobinopathy due to globin chain mutation   127038008
children
hierarchies
a selection of possible paths
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 disease   51053007

ancestors
sorted most to least specific
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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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