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