Congenital fibrinogen abnormality	Hereditary coagulation factor deficiency
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Hereditary factor I deficiency disease (disorder)
	Hereditary factor I deficiency disease
	Hereditary hypofibrinogenemia
	hereditaire stollingsfactor I-deficiëntie
	erfelijke fibrinogeendeficiëntie hereditaire factor I-deficiëntie

Id	31925001
Status	Primitive

Occurrence

Has interpretation	Abnormal
Interprets	Hemostatic function

DHD Diagnosis thesaurus reference set

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

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Congenital afibrinogenemia

Congenital hypofibrinogenemia

Hereditary dysfibrinogenemia1