SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Hereditary persistence of fetal hemoglobin   191201002

SNOMED CT code


SNOMED code191201002
nameHereditary persistence of fetal hemoglobin
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary persistence of fetal hemoglobin (disorder)
synonyms
  • Hereditary persistence of foetal haemoglobin
  • HPFH - Hereditary persistence of foetal haemoglobin
  • Hb F disease
  • HPFH - Hereditary persistence of fetal hemoglobin
  • Hereditary persistence of fetal hemoglobin
  • HPFH - Hereditary persistence of fetal haemoglobin
  • Hereditary persistence of fetal haemoglobin
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parentsHereditary hemoglobinopathy   427306008
childrenHereditary persistence of fetal hemoglobin with sickle cell disease syndrome   783254003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Hereditary persistence of fetal hemoglobin   191201002

ancestors
sorted most to least specific
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