OMIA:000018-9925 : Afibrinogenaemia or hypofibrinogenaemia in Capra hircus

In other species: dog , sheep

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: yes

Considered a defect: yes

Key variant known: no

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:000018-9925: Online Mendelian Inheritance in Animals (OMIA) [dataset].


1972 Breukink, H.J., Hart, H.C., Arkel, C., Veldon, N.A., Watering, C.C. :
Congenital afibrinogenemia in goats Zentralblatt fur Veterinarmedizin 19:661-676, 1972. Pubmed reference: 4628722 .

Edit History

  • Created by Frank Nicholas on 06 Sep 2005