OMIA:000175-9685 : Cerebellar abiotrophy in Felis catus (domestic cat)

In other species: dog , horse , taurine cattle , goat , sheep , Magellanic penguin

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. (2005). OMIA:000175-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset].


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.

2018 Scott, E.Y., Woolard, K.D., Finno, C.J., Murray, J.D. :
Cerebellar abiotrophy across domestic species. Cerebellum 17:372-379, 2018. Pubmed reference: 29294214. DOI: 10.1007/s12311-017-0914-1.
1999 Shamir, M., Perl, S., Sharon, L. :
Late onset of cerebellar abiotrophy in a Siamese cat Journal of Small Animal Practice 40:343-345, 1999. Pubmed reference: 10444756.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005