SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Hereditary hemoglobinopathy due to globin chain mutation  127038008

Hereditary hemoglobin S  416417002

Sickling disorder due to hemoglobin S  417357006

Double heterozygous sickling disorder  23269001

Sickle cell-hemoglobin Lepore disease   127047000

SNOMED CT code


SNOMED code127047000
nameSickle cell-hemoglobin Lepore disease
statusactive
date introduced2002-01-31
fully specified name(s)Sickle cell-hemoglobin Lepore disease (disorder)
synonyms
  • Sickle cell-Hb Lepore disease
  • Sickle cell-hemoglobin Lepore disease
  • Sickle cell-haemoglobin Lepore disease
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parentsDouble heterozygous sickling disorder   23269001
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
            Hereditary hemoglobin S   416417002
              Sickling disorder due to hemoglobin S   417357006
                Double heterozygous sickling disorder   23269001
                  Sickle cell-hemoglobin Lepore disease   127047000

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.

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