SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Hereditary coagulation factor deficiency  16922007

Hereditary factor I deficiency disease   31925001

SNOMED CT code


SNOMED code31925001
nameHereditary factor I deficiency disease
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary factor I deficiency disease (disorder)
synonyms
  • Hereditary hypofibrinogenaemia
  • Hereditary factor I deficiency disease
  • Hereditary hypofibrinogenemia
attributes - group2
Has interpretationAbnormal   263654008
InterpretsHemostatic function   74848003
attributes - group1
OccurrenceCongenital   255399007
parents
  • Hereditary coagulation factor deficiency   16922007
  • Congenital fibrinogen abnormality   234456000
children
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary coagulation factor deficiency   16922007
            Hereditary factor I deficiency disease   31925001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital fibrinogen abnormality   234456000
          Hereditary factor I deficiency disease   31925001

ancestors
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