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OMIA:000401-9615 : Gangliosidosis, generic in Canis lupus familiaris (dog)

In other species: emu , domestic cat , pig , taurine cattle

Categories: Lysosomal storage disease , Nervous system phene

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: Renamed from 'Gangliosidosis' to 'Gangliosidosis, generic' [19/06/2024]. See also entries for specific types of gangliosidosis: OMIA:000402 : Gangliosidosis, GM1;  OMIA:000403 : Gangliosidosis, GM2, generic; OMIA:001427 : Gangliosidosis, GM2, GM2A-related; OMIA:001461 : Gangliosidosis, GM2, type I (B variant); and OMIA:001462 : Gangliosidosis, GM2, type II (Sandhoff or variant 0)

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000401-9615: 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.

1976 Baker, H.J., Mole, J.A., Lindsey, J.R., Creel, R.M. :
Animal models of human ganglioside storage diseases Federation Proceedings 35:1193-1201, 1976. Pubmed reference: 816677.
1970 Gambetti, L.A., Kelly, A.M., Steinberg, S.A. :
Biochemical studies in a canine gangliosidosis. (Abstract) Journal of Neuropathology and Experimental Neurology 29:137-138, 1970.

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  • Created by Frank Nicholas on 06 Sep 2005