OMIA 000468-9913 : Heterochromia irides/iridis in Bos taurus
Category: Vision / eye phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 142500 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Considered a defect: yes
Key variant known: no
Cross-species summary: Difference in colour of the iris in the two eyes, or in different areas of one iris.
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
|1969||Leipold, H.W., Huston, K. :>|
|Histopathology of incomplete albinism and heterochromia irides in the Hereford. Cornell Vet 59:69-75, 1969. Pubmed reference: 5812499.|
|1968||Huston, K., Leipold, H.W., Freeman, A.E. :>|
|Heterochromia irides in dairy cattle. J Dairy Sci 51:1101-2, 1968. Pubmed reference: 5690266. DOI: 10.3168/jds.S0022-0302(68)87133-4.|
|Leipold, H.W., Huston, K. :>|
|Incomplete albinism and heterochromia irides in Herefords Journal of Heredity 59:3-8, 1968. Pubmed reference: 5656916.|
- Created by Frank Nicholas on 06 Sep 2005
- Changed by Frank Nicholas on 18 Oct 2011
- Changed by Frank Nicholas on 02 Dec 2011