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

Categories: Haematopoietic system phene

Possibly relevant human trait(s) and/or gene(s) (MIM number): 176860 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Considered a defect: yes

Key variant known: no

Species-specific name: Hypercoaguable state

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). 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