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].


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