OMIA:001461-9986 : Gangliosidosis, GM2, type I (B variant) in Oryctolagus cuniculus |
In other species: muntjak , American flamingo , sheep , dog , pig
Categories: Lysosomal storage disease
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 272800 (trait) , 606869 (gene)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Tay-Sachs disease
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
Reference
| 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