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OMIA:000018-9940 : Afibrinogenaemia or hypofibrinogenaemia in Ovis aries (sheep)

In other species: dog , goat

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

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

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