SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary factor IX deficiency disease  41788008

Hereditary factor IX deficiency disease with inhibitor   438372000

SNOMED CT code


SNOMED code438372000
nameHereditary factor IX deficiency disease with inhibitor
statusactive
date introduced2009-01-31
fully specified name(s)Hereditary factor IX deficiency disease with inhibitor (disorder)
synonyms
  • Haemophilia B with inhibitor
  • Hemophilia B with inhibitor
  • Hereditary factor IX deficiency disease with inhibitor
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
attributes - group2
OccurrenceCongenital   255399007
parentsHereditary factor IX deficiency disease   41788008
children
  • Mild hereditary factor IX deficiency disease with inhibitor   440868005
  • Moderate hereditary factor IX deficiency disease with inhibitor   440867000
  • Severe hereditary factor IX deficiency disease with inhibitor   440866009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary factor IX deficiency disease   41788008
          Hereditary factor IX deficiency disease with inhibitor   438372000

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