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 R├ęsibois, 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