Categories: Haematopoietic system phene

Possible human homologues (MIM numbers): 264900 (gene) , 612416 (trait)

Links to relevant human diseases in MONDO:

• MONDO:0012897: congenital factor XI deficiency

Cross-species summary: Congenital factor XI deficiency / F11 deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery. [Orphanet : 329] The disease is also called plasma thromboplastin antecedent (PTA) deficiency, haemophilia C, or Rosenthal syndrome.

Species in which this phene is found:
dog (Canis lupus familiaris)
domestic cat (Felis catus)
taurine cattle (Bos taurus)