OMIA:000335-9796 : Encephalomyelopathy in Equus caballus (horse)

In other species: dog , domestic cat , sheep

Categories: Nervous system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 161700 (trait) , 270900 (trait)

Mendelian trait/disorder: unknown

Considered a defect: yes

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2024). OMIA:000335-9796: 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.

2024 Durward-Akhurst, S.A., Marlowe, J.L., Schaefer, R.J., Springer, K., Grantham, B., Carey, W.K., Bellone, R.R., Mickelson, J.R., McCue, M.E. :
Predicted genetic burden and frequency of phenotype-associated variants in the horse. Sci Rep 14:8396, 2024. Pubmed reference: 38600096. DOI: 10.1038/s41598-024-57872-8.
2019 Marquardt, S.A., Wilcox, C.V., Burns, E.N., Peterson, J.A., Finno, C.J. :
Previously identified genetic variants in ADGRL3 are not associated with risk for equine degenerative myeloencephalopathy across breeds. Genes (Basel) 10, 2019. Pubmed reference: 31491999. DOI: 10.3390/genes10090681.
1991 Seahorn, T.L., Fuentealba, I.C., Illanes, O.G., Storts, R.W. :
Congenital Encephalomyelopathy in a Quarter Horse Equine Veterinary Journal 23:394-396, 1991. Pubmed reference: 1959534.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Imke Tammen2 on 04 Jun 2024