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

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

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

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2013). OMIA:001461-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset].


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