OMIA:000740-9685 : Olivopontocerebellar atrophy in Felis catus (domestic cat) |
Categories: Nervous system phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 164400 (trait) , 183090 (trait) , 258300 (trait) , 164500 (trait) , 302500 (trait) , 164700 ()
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Abbreviated to OPCA. Also called Olivopontocerebellar hypoplasia.
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. (2011). OMIA:000740-9685: 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.
| 2004 | Résibois, A., Poncelet, L. : |
| Olivopontocerebellar atrophy in two adult cats, sporadic cases or new genetic entity. Vet Pathol 41:20-9, 2004. Pubmed reference: 14715964. DOI: 10.1354/vp.41-1-20. | |
| 1946 | Schut, J.W. : |
| Olivopontocerebellar atrophy in a cat. J Neuropathol Exp Neurol 5:77-81, 1946. Pubmed reference: 21010608. | |
| 1934 | Brouwer, B.A. : |
| Familial olivo-ponto-cerebellar hypoplasia in cats Psychiatrische en Neurologische Bladen 38:352-367, 1934. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005
- Changed by Frank Nicholas on 26 Oct 2011