OMIA:000018-9925 : Afibrinogenaemia or hypofibrinogenaemia in Capra hircus |
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]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
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