OMIA:002776-452646 : Sex chromosome difference of sexual development, generic in Neovison vison (American mink) |
In other species: dog , domestic cat , horse , pig , taurine cattle , goat , sheep , gray short-tailed opossum , wood lemming , water buffalo
Categories: Reproductive system phene , Chromosomal disorder
Links to MONDO diseases:
Mendelian trait/disorder: no
Considered a defect: yes
Key variant known: no
Cross-species summary: This is a group of differences of sexual development (DSD) due to abnormal sex chromosome constitutions (e.g., monosomy; trisomy; mosaicism) (adopted from MESH:D058533)
Species-specific name: Previously listed as OMIA:000564-452646 [01/10/2023]
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. (2023). OMIA:002776-452646: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 1966 | Nes, N. : |
| Diploid-triploid chimerism in a true hermaphrodite mink (Mustela vison) Hereditas 56:159-170, 1966. |
Edit History
- Created by Imke Tammen2 on 01 Oct 2023
- Changed by Imke Tammen2 on 01 Oct 2023