OMIA:001461-9986 : Gangliosidosis, GM2, type I (B variant) in Oryctolagus cuniculus (rabbit)

In other species: American flamingo , dog , pig , muntjak , taurine cattle , sheep

Categories: Lysosomal storage disease , Nervous system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 272800 (trait) , 606869 (gene)

Single-gene trait/disorder: unknown

Disease-related: yes

Cross-species summary: Tay-Sachs disease

Contact us

If you notice anything missing or in need of change, please contact us at: [email protected].

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2013). OMIA:001461-9986: 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.

2026 Suarez, D.A., Leal, A.F., Pachajoa, H., Granados-Villalobos, S., Espejo-Mojica, A.J., Seyrantepe, V., Alméciga-Díaz, C.J. :
Tay-Sachs disease models: From cellular and animal models to treatment perspectives. Mol Genet Metab 148:S1096-7192(26)00188-5:109905, 2026. Pubmed reference: 41880697. DOI: 10.1016/j.ymgme.2026.109905.
2013 Rickmeyer, T., Schöniger, S., Petermann, A., Harzer, K., Kustermann-Kuhn, B., Fuhrmann, H., Schoon, H.A. :
GM2 gangliosidosis in an adult pet rabbit. J Comp Pathol 148:243-7, 2013. Pubmed reference: 22878054. DOI: 10.1016/j.jcpa.2012.06.008.

Edit History


  • Created by Frank Nicholas on 03 May 2013