OMIA:000018-9940 : Afibrinogenaemia or hypofibrinogenaemia in Ovis aries |
Categories: Haematopoietic system phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 202400 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: In combining these two disorders in the one entry, OMIA is following the practice of the corresponding entry for humans in OMIM
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000018-9940: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 1997 | Fecteau, G., Zinkl, J.G., Smith, B.P., Oneil, S., Smith, S., Klopfer, S. : |
| Dysfibrinogenemia or afibrinogenemia in a border leicester lamb Canadian Veterinary Journal - Revue Veterinaire Canadienne 38:443-444, 1997. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005