D68.20 Carence héréditaire en facteur I

Meta Para295: P Para301: P MortL1Code: 1-050 MortL2Code: 2-072 MortL3Code: 3-022 MortL4Code: 4-018 MortBCode: 099 SexCode: 9 SexReject: 9 AgeLowDiff: 999 AgeLow: 9999 AgeHighDiff: 999 AgeHigh: 9999 AgeReject: 9 RareDisease: N Content: J Infectious: N EBMLabor: N

inclusion Afibrinogénémie congénitale Dysfibrinogénémie (congénitale) Carence en fibrinogènele