OMIA 000018-9925 : Afibrinogenaemia or hypofibrinogenaemia in Capra hircus |
In other species:
dog
,
sheep
Possibly relevant human trait(s) and/or gene(s) (MIM number):
202400 (trait)
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
Reference
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