OMIA:000715-9685 : Neuroaxonal dystrophy, generic in Felis catus (domestic cat)

In other species: dog , horse , sheep , rabbit

Categories: Nervous system phene

Possibly relevant human trait(s) and/or gene(s) (MIM number): 608507 (gene)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: Progressive ataxia, hypermetria, proprioceptive deficits, head incoordination and tremors.

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:000715-9685: 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.

1996 Rodriguez, F., Delosmonteros, A.E., Morales, M., Herraez, P., Jaber, J.R., Fernandez, A. :
Neuroaxonal dystrophy in two siamese kitten littermates Veterinary Record 138:548-549, 1996. Pubmed reference: 8782363.
1993 Carmichael, K.P., Howerth, E.W., Oliver, J.E., Klappenbach, K. :
Neuroaxonal Dystrophy in a Group of Related Cats Journal of Veterinary Diagnostic Investigation 5:585-590, 1993. Pubmed reference: 8286459.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005