afwijking van fibrinogeen	congenitale ziekte
\|	\|

congenitale afwijking van fibrinogeen (aandoening)
	congenitale afwijking van fibrinogeen
	congenitale afwijking van stollingsfactor I
	Congenital fibrinogen abnormality

Id	234456000
Status	Defined

Occurrence

Has interpretation	afwijkend
Interprets	hemostase

SNOMED CT to ICD-10 extended map

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

|

dysfibrinogenemie4

hereditaire stollingsfactor I-deficiëntie4