OMIA:001353 : Scott Syndrome

Categories: Haematopoietic system phene

Possible human homologues (MIM numbers): 262890 (trait) , 608663 (gene)

Links to relevant human diseases in MONDO:

Cross-species summary: Bleeding abnormality due to deficiency of platelet binding of factor X

Species in which this phene is found:
dog (Canis lupus familiaris)

Edit History


  • Created by Frank Nicholas on 03 Nov 2010
  • Changed by Frank Nicholas on 23 Apr 2013
  • Changed by Frank Nicholas on 08 Nov 2016
  • Changed by Imke Tammen2 on 17 Apr 2021
  • Changed by Imke Tammen2 on 06 Jul 2021
  • Changed by Imke Tammen2 on 01 Sep 2021
  • Changed by Imke Tammen2 on 23 Jan 2023