OMIA:000366-9685 : Fanconi syndrome in Felis catus (domestic cat)

In other species: dog , horse , taurine cattle

Categories: Renal / urinary system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 227810 (trait) , 138160 (gene)

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: Also known as Fanconi-Bickel Syndrome (FBS)

Breed: Sphynx (Cat) (VBO_0100230).
Breeds in which the phene has been documented. (If a likely causal variant has been documented for the phene, see the variant table breeds in which the variant has been reported).

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:000366-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset].


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