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ICD2021
Klassifikation bearbeiten
Overview
III
D65-D69
D68
D68.2
D68.20
Description
Hereditärer Faktor-I-Mangel
Coding
No available coding.
Additional information
TEXT
inclusion: Angeborene Afibrinogenämie
TEXT
inclusion: Dysfibrinogenämie (angeboren)
TEXT
inclusion: Fibrinogen-Mangel
D68.21
Description
Hereditärer Faktor-II-Mangel
Coding
No available coding.
Additional information
TEXT
inclusion: Prothrombin-Mangel
D68.22
Description
Hereditärer Faktor-V-Mangel
Coding
No available coding.
Additional information
TEXT
inclusion: Labiler-Faktor-Mangel
TEXT
inclusion: Owren-Krankheit
TEXT
inclusion: Plasma-Ac-Globulin-Mangel
TEXT
inclusion: Proakzelerin-Mangel
D68.23
Description
Hereditärer Faktor-VII-Mangel
Coding
No available coding.
Additional information
TEXT
inclusion: Hypoprokonvertinämie
TEXT
inclusion: Prokonvertin-Mangel
TEXT
inclusion: Stabiler-Faktor-Mangel
D68.24
Description
Hereditärer Faktor-X-Mangel
Coding
No available coding.
Additional information
TEXT
inclusion: Stuart-Prower-Faktor-Mangel
D68.25
Description
Hereditärer Faktor-XII-Mangel
Coding
No available coding.
Additional information
TEXT
inclusion: Hageman-Faktor-Mangel
D68.26
Description
Hereditärer Faktor-XIII-Mangel
Coding
No available coding.
Additional information
TEXT
inclusion: Fibrinstabilisierender-Faktor-Mangel
D68.28
Description
Hereditärer Mangel an sonstigen Gerinnungsfaktoren
Coding
No available coding.
Additional information
No additional information available.