Autosomal hereditary disorder	Congenital fibrinogen abnormality	Fibrinogen deficiency
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Hypodysfibrinogenemia (disorder)
	Hypodysfibrinogenemia
	hypodysfibrinogenemie

Id	234458004
Status	Primitive

Occurrence

Has interpretation	Abnormal
Interprets	Hemostatic function

ICD-10 complex map reference set

Target	D68.2
Rule	TRUE
Advice	ALWAYS D68.2
Correlation	SNOMED CT source code to target map code correlation not specified