OMIA:001127-9615 : Otocephaly, generic in Canis lupus familiaris (dog)

In other species: taurine cattle

Categories: Craniofacial phene

Possibly relevant human trait(s) and/or gene(s) (MIM number): 202650 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

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. (2011). OMIA:001127-9615: 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.

2006 Martínez, J.S., Velázquez, I.R., Reyes, H., Fajardo, R. :
Congenital holoprosencephaly with severe otocephaly in a rottweiler puppy. Vet Rec 158:518-9, 2006. Pubmed reference: 16617045.
1964 Fox, M.W. :
Anatomy of the Canine Skull in Low-grade Otocephaly. Can J Comp Med Vet Sci 28:105-7, 1964. Pubmed reference: 17649505.
1963 Fox, M.W. :
Low-grade otocephaly in a dog J Am Vet Med Assoc 143:289-90, 1963. Pubmed reference: 14042920.
Fox, M.W. :
Developmental Abnormalities of the Canine Skull. Can J Comp Med Vet Sci 27:219-22, 1963. Pubmed reference: 17649461.

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  • Created by Frank Nicholas on 26 Oct 2011