OMIA:002657-9685 : Chromosomal abnormality, generic in Felis catus (domestic cat) |
In other species: salmonids , rainbow trout , Mallard , domestic goose , rock pigeon , chicken , chukar partridge , common quail , turkey , gray wolf , dog , red fox , ass (donkey) , onager , domestic horse , pig , red deer , reindeer , aoudad , taurine cattle , goat , brindled gnu , sheep , rabbit , raccoon dog , Barbary partridge , black wildebeest , Volga pikeperch , plains zebra , water buffalo , Japanese quail , kiang , Houbara bustard , mule , American mink , Arctic fox
Categories: Chromosomal disorder
Single-gene trait/disorder: unknown
Disease-related: yes
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Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:002657-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2023 | Szczerbal, I., Nowacka-Woszuk, J., Rozynek, J., Stachowiak, M., Switonski, M. : |
| X monosomy in a British shorthair cat with skeletal abnormalities and behavioral problems. Anim Genet 54:655-656, 2023. Pubmed reference: 37380359. DOI: 10.1111/age.13343. |
Edit History
- Created by Imke Tammen2 on 17 Jul 2023