OMIA:000819-9796 : Prekallikrein deficiency in Equus caballus (horse)

In other species: dog

Categories: Haematopoietic system phene

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 229000 (gene) , 612423 (trait)

Links to MONDO diseases:

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: In humans also called Fletcher factor deficiency

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000819-9796: Online Mendelian Inheritance in Animals (OMIA) [dataset].


Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.

2021 Dahlgren, A.R., Tablin, F., Finno, C.J. :
Genetics of equine bleeding disorders. Equine Vet J 53:30-37, 2021. Pubmed reference: 32463964 . DOI: 10.1111/evj.13290.
1990 Geor, R.J., Jackson, M.L., Lewis, K.D., Fretz, P.B. :
Prekallikrein deficiency in a family of Belgian horses. Journal of the American Veterinary Medical Association 197:741-745, 1990. Pubmed reference: 2211324 .
1986 Turrentine, M.A., Sculley, P.W., Green, E.M., Johnson, G.S. :
Prekallikrein deficiency in a family of miniature horses American Journal of Veterinary research 47:2464-2467, 1986. Pubmed reference: 3641551 .

Edit History

  • Created by Frank Nicholas on 06 Sep 2005