SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital fibrinogen abnormality  234456000

Hereditary factor I deficiency disease  31925001

Congenital hypofibrinogenemia   439145006

SNOMED CT code


SNOMED code439145006
nameCongenital hypofibrinogenemia
statusactive
date introduced2009-01-31
fully specified name(s)Congenital hypofibrinogenemia (disorder)
synonyms
  • Congenital hypofibrinogenemia
  • Congenital hypofibrinogenaemia
attributes - group2
Has interpretationAbnormal   263654008
InterpretsHemostatic function   74848003
attributes - group1
OccurrenceCongenital   255399007
parentsHereditary factor I deficiency disease   31925001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital fibrinogen abnormality   234456000
          Hereditary factor I deficiency disease   31925001
            Congenital hypofibrinogenemia   439145006

ancestors
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