OMIA:000625-9844 : Mannosidosis, alpha in Lama glama (llama) |
In other species: dog , domestic cat , taurine cattle , goat , sheep , domestic guinea pig
Categories: Lysosomal storage disease
Links to possible relevant human trait(s) and/or gene(s) in OMIM: 248500 (trait) , 609458 (gene)
Links to relevant human diseases in MONDO:
Single-gene trait/disorder: unknown
Disease-related: unknown
Cross-species summary: A lysosomal storage disease in which there is a buildup (storage) of mannose-rich compounds, due to the lack of the enzyme alpha-mannosidase, whose task is to cleave mannose from such compounds. Clinical signs include ataxia, head tremor, aggression, and finally paralysis and death.
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Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2025). OMIA:000625-9844: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
References
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 | Marin, R.E., Uzal, F.A. : |
| Lisosomal storage disease caused by ingestion of Astragalus spp in llamas: an emergent concern. Vet Res Commun 48:1999-2005, 2024. Pubmed reference: 38758424. DOI: 10.1007/s11259-024-10397-x. | |
| 2020 | Marin, R.E., Micheloud, J.F., Vignale, N.D., Gimeno, E.J., O'Toole, D., Gardner, D.R., Woods, L., Uzal, F.A. : |
| Intoxication by <i>Astragalus garbancillo</i> var. <i>garbancillo</i> in llamas. J Vet Diagn Invest 32:467-470, 2020. Pubmed reference: 32233843. DOI: 10.1177/1040638720914338. |
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- Created by Frank Nicholas on 09 Jun 2025