SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital fibrinogen abnormality  234456000

Dysfibrinogenemia  111589005

Congenital dysfibrinogenemia   45366001

SNOMED CT code


SNOMED code45366001
nameCongenital dysfibrinogenemia
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary dysfibrinogenemia (disorder)
synonyms
  • Hereditary dysfibrinogenaemia
  • Hereditary dysfibrinogenemia
  • Congenital dysfibrinogenaemia
  • Congenital dysfibrinogenemia
attributes - group2
Has interpretationAbnormal   263654008
InterpretsHemostatic function   74848003
attributes - group1
OccurrenceCongenital   255399007
parents
childrenHereditary thrombophilic dysfibrinogenemia   438827002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital fibrinogen abnormality   234456000
          Dysfibrinogenemia   111589005
            Congenital dysfibrinogenemia   45366001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital fibrinogen abnormality   234456000
          Hereditary factor I deficiency disease   31925001
            Congenital dysfibrinogenemia   45366001

ancestors
sorted most to least specific
cpt crosswalks

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