OMIA:001418-9615 : Cricopharyngeal dysfunction in Canis lupus familiaris (dog) |
Categories: Digestive / alimentary phene
Single-gene trait/disorder: yes
Mode of inheritance: Autosomal recessive
Disease-related: yes
Key variant known: no
Species-specific name: CD
Species-specific description: As reported by Davidson et al. (2004), "The CD phenotype was determined by videofluoroscopy, and dogs were classified as affected if the upper esophageal sphincter (UES) did not open, if there were morphologic abnormalities of the UES, or if opening of the UES was delayed for > or = 6 videofluoroscopic frames (0.2 seconds) after closure of the epiglottis."
Breed:
Golden Retriever (Dog) (VBO_0200610).
Breeds in which the phene or likely causal variants have been documented. If a likely causal variant has been documented, see variant-specific breed information in the variant table. (Breed information may be incomplete).
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Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2022). OMIA:001418-9615: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
2004 | Davidson, AP., Pollard, RE., Bannasch, DL., Marks, SL., Hornof, WJ., Famula, TR. : |
Inheritance of cricopharyngeal dysfunction in Golden Retrievers. Am J Vet Res 65:344-9, 2004. Pubmed reference: 15027684. |
Edit History
- Created by Frank Nicholas on 25 Oct 2005
- Changed by Frank Nicholas on 18 Jun 2013
- Changed by Imke Tammen2 on 23 Oct 2022