OMIA:001290-9796 : Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome in Equus caballus (horse) |
Categories: Homeostasis / metabolism phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 238970 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Breed:
Morgan (Horse) (VBO_0001022).
Breeds in which the phene has been documented. For breeds in which a likely causal variant has been documented, see the variant table below
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2022). OMIA:001290-9796: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 1997 | McConnico, R.S., Duckett, W.M., Wood, P.A. : |
| Persistent hyperammonemia in two related Morgan weanlings Journal of Veterinary Internal Medicine 11:264-266, 1997. Pubmed reference: 9298483 . |
Edit History
- Created by Frank Nicholas on 06 Sep 2005
- Changed by Imke Tammen2 on 23 Oct 2022