OMIA:000965-9986 : Syringomyelia in Oryctolagus cuniculus
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).
Cite this entry
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.|
- Changed by Frank Nicholas on 03 May 2016
- Created by Frank Nicholas on 03 May 2016