SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Homozygous hemoglobinopathy  123772008

Hb S disease   127040003

SNOMED CT code


SNOMED code127040003
nameHb S disease
statusactive
date introduced2002-01-31
fully specified name(s)Sickle cell-hemoglobin SS disease (disorder)
synonyms
  • Hemoglobin S-S disease
  • Drepanocythemia
  • Hb SS disease
  • Hereditary hemoglobinopathy disorder homozygous for hemoglobin S
  • Sickle cell anemia
  • Sickle cell-hemoglobin SS disease
  • Sickle cell-haemoglobin SS disease
  • Hereditary haemoglobinopathy disorder homozygous for haemoglobin S
  • Drepanocythaemia
  • Sickle cell anaemia
  • Haemoglobin S disease
  • Haemoglobin S-S disease
  • Hemoglobin S disease
  • Hb S disease
attributes - group1
InterpretsMeasurement of total hemoglobin concentration   441689006
Has interpretationBelow reference range   281300000
attributes - group5
Causative agentHemoglobin S   50095005
attributes - group4
Associated morphologyDrepanocyte   49938009
attributes - group3
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
  • Homozygous hemoglobinopathy   123772008
  • Anemia due to disturbance of hemoglobin synthesis   14514008
  • Anemia due to intrinsic red cell abnormality   323666000
  • Sickling disorder due to hemoglobin S   417357006
children
  • [X]Other sickle cell disorders   191419008  removed: 2009-01-31
  • Hemoglobin SS disease with crisis   417425009
  • Hemoglobin SS disease without crisis   416180004
  • Sickle cell anemia in mother complicating childbirth   10759351000119103
  • Sickle cell anemia NOS   191199004  removed: 2010-01-31
  • Sickle cell anemia of unspecified type   191195005  removed: 2010-01-31
  • Sickle cell anemia with coexistent alpha-thalassemia   127045008
  • Sickle cell anemia with crisis   191197002  removed: 2005-07-31
  • Sickle cell anemia with high hemoglobin F   234391009
  • Sickle cell anemia with no crisis   191196006  removed: 2005-07-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Homozygous hemoglobinopathy   123772008
            Hb S disease   127040003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Anemia   271737000
          Anemia due to disturbance of hemoglobin synthesis   14514008
            Hb S disease   127040003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Anemia   271737000
          Anemia due to intrinsic red cell abnormality   323666000
            Hb S disease   127040003

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
                Hb S disease   127040003

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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