You are here: OMIA / Search / OMIA:000835 / horse

OMIA:000835-9796 : Protein C deficiency in Equus caballus (horse)

Categories: Haematopoietic system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 176860 (trait)

Mendelian trait/disorder: yes

Disease-related: yes

Key variant known: no

Species-specific name: Hypercoaguable state

Breed: Thoroughbred (Horse) (VBO_0001083).
Breeds in which the phene has been documented. (If a likely causal variant has been documented for the phene, see the variant table breeds in which the variant has been reported).

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2024). OMIA:000835-9796: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1993 Edens, L.M., Morris, D.D., Prasse, K.W., Anver, M.R. :
Hypercoagulable state associated with a deficiency of protein C in a thoroughbred colt. J Vet Intern Med 7:190-3, 1993. Pubmed reference: 8331614. DOI: 10.1111/j.1939-1676.1993.tb03185.x.

Edit History


  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Imke Tammen2 on 15 Jun 2024