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].


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