Alpha thalassemia   68913001

SNOMED CT code


SNOMED code68913001
nameAlpha thalassemia
statusactive
date introduced2002-01-31
fully specified name(s)Alpha thalassemia (disorder)
synonyms
  • Alpha thalassemia
  • Alpha thalassaemia
  • alpha thalassemia
  • alpha thalassaemia
  • Alpha thalassaemia syndrome
  • Alpha thalassemia syndrome
attributes - group2
InterpretsMeasurement of total hemoglobin concentration   441689006
Has interpretationBelow reference range   281300000
attributes - group3
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parentsThalassemia   40108008
children
  • Alpha plus thalassemia   36467003
  • Alpha thalassemia trait   234384006  removed: 2004-07-31
  • Alpha thalassemia X-linked intellectual disability syndrome   715342005
  • Alpha thalassemia-2 trait   234385007
  • Alpha trait thalassemia   191187006
  • Alpha zero thalassemia   66055002
  • Alpha-thalassemia intellectual disability syndrome linked to chromosome 16   734349003
  • Hemoglobin Bart's hydrops syndrome   5300004
  • Hemoglobin Constant Spring trait   234386008
  • Hemoglobin H constant spring thalassemia   447117006
  • Hemoglobin H disease   48553001
  • Hemoglobin Paksé disease   1148897000
  • Hemoglobin Seal Rock disease   1148899002
  • Homozygous alpha thalassemia   234383000
  • Sickle cell anemia with coexistent alpha-thalassemia   127045008
  • Sickle cell trait with coexistent alpha-thalassemia   127046009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Thalassemia   40108008
            Alpha thalassemia   68913001

ancestors
sorted most to least specific
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