Congenital factor XI deficiency

Orpha code: 329OMIM code: 612416

Definition

A rare inherited bleeding disorder characterized by reduced levels and/or activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery.

Disease data
Classification

Disease

Synonyms
Hemophilia C
Hemofilia C
Niedobór czynnika przeciwhemofilowego C
Niedobór czynnika Rosenthala
Niedobór PTA
Zespół Rosenthala
PTA deficiency
Plasma thromboplastin antecedent deficiency
Rosenthal factor deficiency
Rosenthal syndrome
ORPHA code
329
OMIM code
612416
ICD10 code
D68.1
ICD11 code
3B13

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl