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OMIA:000965-9986 : Syringomyelia in Oryctolagus cuniculus (rabbit)

In other species: dog , domestic cat , horse , taurine cattle

Categories: Nervous system phene

Possibly relevant human trait(s) and/or gene(s) (MIM number): 186700 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: no

Mode of inheritance: Multifactorial

Considered a defect: yes

Key variant known: no

Cross-species summary: Disorder in which a fluid-filled cyst (called a syrinx) forms within the spinal cord

Species-specific description: See Robinson (1958, p. 335-336).

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. (2016). OMIA:000965-9986: 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.

1958 Robinson, R. :
Genetic studies of the rabbit. Bibliographia Genetica 17:229–558, 1958.
1937 Nachtsheim, H. :
Erbpathologische Untersuchungen am Kaninchen [Investigation of inherited defects in rabbits] Z. indo Abst. u. Vererbgs 73:463-466, 1937. DOI: 10.1007/BF01847500.

Edit History


  • Created by Frank Nicholas on 03 May 2016
  • Changed by Frank Nicholas on 03 May 2016