OMIA:000189-9986 : Chondrodystrophy in Oryctolagus cuniculus (rabbit)
Categories: Skeleton phene (incl. short stature & teeth)
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Considered a defect: yes
Key variant known: no
Species-specific symbol: cd
History: This form of disproportionate dwarfism was first reported by Fox and Crary (1971).
Have human generated variants been created, e.g. through genetic engineering and gene editing
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.
|1981||Webber, R.J., Fox, R.R., Sokoloff, L. :|
|In vitro culture of rabbit growth plate chondrocytes. 2. Chondrodystrophic mutants. Growth 45:269-78, 1981. Pubmed reference: 6458543.|
|1975||Fox, R.R., Crary, D.D. :|
|Hereditary chondrodystrophy in the rabbit. Genetics and pathology of a new mutant, a model for metatropic dwarfism. J Hered 66:271-6, 1975. Pubmed reference: 1184951.|
|1971||Fox, R.R., Crary, D.D. :|
|A new recessive chondrodystrophy in the rabbit Teratology 4:245-246, 1971.|
- Created by Frank Nicholas on 06 Sep 2005
- Changed by Frank Nicholas on 05 Oct 2011
- Changed by Frank Nicholas on 28 Apr 2016
- Changed by Frank Nicholas on 29 Apr 2016