OMIA:000933-9986 : Spina bifida in Oryctolagus cuniculus (rabbit)

In other species: dog , domestic cat , taurine cattle , sheep , snow leopard

Categories: Embryo phene

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 182940 (trait) , 183802 (trait) , 301410 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: A neural tube defect (NTD) characterised by defective closure of the two halves of the vertebral arch through which the spinal cord and meninges may or may not protrude.

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. (2005). OMIA:000933-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

References

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.

2021 Zarzycki, A., Thomas, Z.M., Mazrier, H. :
Comparison of inherited neural tube defects in companion animals and livestock. Birth Defects Res 113:319-348, 2021. Pubmed reference: 33615733. DOI: 10.1002/bdr2.1848.
1966 Crary, D.D., Fox, R.R., Sawin, P.B. :
Spina bifida in the rabbit. J Hered 57:236-43, 1966. Pubmed reference: 5339481.
1937 Nachtsheim, H. :
Erbpathologische Untersuchungen am Kaninchen [Investigation of inherited defects in rabbits] Z. indo Abst. u. Vererbgs 73:463-466, 1937. DOI: 10.1007/BF01847500.

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  • Created by Frank Nicholas on 06 Sep 2005