OMIA:000366-9685 : Fanconi syndrome in Felis catus (domestic cat) |
In other species: dog , horse , taurine cattle
Categories: Renal / urinary system phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 227810 (trait) , 138160 (gene)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Also known as Fanconi-Bickel Syndrome (FBS)
Genetic engineering:
Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing
Breed:
Sphynx (Cat) (VBO_0100230).
Breeds in which the phene has been documented. For breeds in which a likely causal variant has been documented, see the variant table below
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:000366-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
2023 | Cˇerná, P., Botts, M.M., Williams, M., Aboellail, T.A., Shropshire, S. : |
Fanconi syndrome with hepatorenal karyomegaly in a young Sphynx cat. JFMS Open Rep 9:20551169231190611, 2023. Pubmed reference: 37810577. DOI: 10.1177/20551169231190611. |
Edit History
- Created by Imke Tammen2 on 15 Oct 2023