OMIA:000487-10036 : Hydrocephalus in Mesocricetus auratus
Categories: Nervous system phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 109400 (trait) , 112240 (trait) , 123155 (trait) , 209970 (trait) , 236600 (trait) , 236635 (trait) , 236640 (trait) , 236660 (trait) , 236670 (trait) , 236690 (trait) , 273730 (trait) , 276950 (trait) , 307000 (trait) , 307010 (trait) , 314390 (trait) , 123155 (trait) , 600257 (trait) , 600559 (trait) , 600991 (trait) , 615181 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Considered a defect: yes
Key variant known: no
Cross-species summary: Enlargement of the cranium caused by accumulation of fluid.
Cite this entry
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.
|2006||Edwards, J.F., Gebhardt-Henrich, S., Fischer, K., Hauzenberger, A., Konar, M., Steiger, A. :|
|Hereditary hydrocephalus in laboratory-reared golden hamsters (Mesocricetus auratus). Vet Pathol 43:523-9, 2006. Pubmed reference: 16846994 . DOI: 10.1354/vp.43-4-523.|
|1972||Yoon, C.H., Slaney, J. :|
|Hydrocephalus : A new mutation in the Syrian golden hamster Journal of Heredity 36:344-346, 1972.|
- Created by Frank Nicholas on 06 Sep 2005
- Changed by Frank Nicholas on 24 Oct 2011
- Changed by Imke Tammen2 on 17 Sep 2022