HPFH A gamma beta^+^ thalassemia   39586009

SNOMED CT code


SNOMED code39586009
nameHPFH A gamma beta^+^ thalassemia
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder)
synonyms
  • Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia
  • Hereditary persistence of foetal haemoglobin (HPFH) A gamma beta^+^ thalassaemia
  • Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia
  • Hereditary persistence of fetal haemoglobin A gamma beta^+^ thalassaemia
  • HPFH A gamma beta^+^ thalassaemia
  • HPFH A gamma beta^+^ thalassemia
attributes - group2
InterpretsMeasurement of total hemoglobin concentration   441689006
Has interpretationBelow reference range   281300000
attributes - group3
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
  • Hereditary persistence of fetal hemoglobin thalassemia   16964007
  • Beta plus thalassemia   79592006
childrenA>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis   5967006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Thalassemia   40108008
            Hereditary persistence of fetal hemoglobin thalassemia   16964007
              HPFH A gamma beta^+^ thalassemia   39586009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Thalassemia   40108008
            Beta thalassemia   65959000
              Beta plus thalassemia   79592006
                HPFH A gamma beta^+^ thalassemia   39586009

ancestors
sorted most to least specific
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