OMIA:001795-9654 : Niemann-Pick disease, type A in Procyon lotor (raccoon) |
In other species: dog , domestic cat , taurine cattle
Categories: Lysosomal storage disease
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 257200 (trait) , 607608 (gene)
Links to MONDO diseases:
Mendelian trait/disorder: unknown
Considered a defect: yes
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:001795-9654: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2013 | Vapniarsky, N., Wenger, D.A., Scheenstra, D., Mete, A. : |
| Sphingomyelin Lipidosis (Niemann-Pick Disease) in a Juvenile Raccoon (Procyon lotor). J Comp Pathol , 2013. Pubmed reference: 23582974. DOI: 10.1016/j.jcpa.2013.01.011. |
Edit History
- Created by Frank Nicholas on 03 May 2013