OMIA:000175-37081 : Cerebellar abiotrophy in Spheniscus magellanicus (Magellanic penguin) |
In other species: dog , domestic cat , horse , taurine cattle , goat , sheep
Categories: Nervous system phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 600224 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Also known as neonatal cerebellar cortical degeneration (NCCD)
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. (2023). OMIA:000175-37081: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2019 | Ioannidis, M., Tanaka, M., Yasui, S., Kezuka, C., Oyamada, M., Hasegawa, T., Izawa, T., Yamate, J., Kuwamura, M. : |
| Late onset of cerebellar cortical degeneration in a Magellanic penguin (Spheniscus magellanicus). J Vet Med Sci 81:750-752, 2019. Pubmed reference: 30956256. DOI: 10.1292/jvms.19-0089. |
Edit History
- Created by Imke Tammen2 on 10 Nov 2023
- Changed by Imke Tammen2 on 10 Nov 2023