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OMIA:001465-9940 : Arthrogryposis multiplex congenita, generic in Ovis aries (sheep)

In other species: pig , taurine cattle

Categories: Skeleton phene (incl. short stature & teeth)

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive lethal

Considered a defect: yes

Key variant known: no

Cross-species summary: conditions involving multiple joint contractures (or stiffness)

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. (2010). OMIA:001465-9940: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

2010 Tejedor, MT., Ferrer, LM., Monteagudo, LV., Ramos, JJ., Lacasta, D., Climent, S. :
Ovine heritable arthrogryposis multiplex congenita with probable lethal autosomal recessive mutation. J Comp Pathol 143:14-9, 2010. Pubmed reference: 20153865. DOI: 10.1016/j.jcpa.2009.12.015.

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  • Created by Frank Nicholas on 16 Nov 2010