OMIA:000540-9986 : Hypotrichosis, generic in Oryctolagus cuniculus (rabbit)

In other species: macaques , dog , domestic cat , pig , taurine cattle , sheep , golden hamster , Mongolian gerbil , meadow voles , domestic guinea pig , American mink

Categories: Integument (skin) phene

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 146520 (trait) , 146550 (trait) , 183849 (trait) , 211370 (trait) , 246500 (trait) , 250460 (trait) , 278200 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: Also known as Hairless

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:000540-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1956 Guenther, F. :
[Hereditary developmental anomalies of the ectoderm - keratosis, hypotrichosis and eye diseases - in rabbits.] Erbliche Entwicklungsanomalien des ausseren Keimblattes beim Kaninchen Keratose - Hypotrichose - Augenleiden Berliner und Munchener Tierarztliche Wochenschrift 69:214-215, 1956.

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  • Created by Frank Nicholas on 06 Sep 2005