OMIA:000181-9544 : Neuronal Ceroid Lipofuscinosis, generic in Macaca mulatta (Rhesus monkey) |
In other species: Mallard , crab-eating macaque , dog , domestic ferret , domestic cat , domestic horse , pig , taurine cattle , goat , sheep , peach-faced lovebird
Categories: Lysosomal storage disease , Nervous system phene
Single-gene trait/disorder: unknown
Disease-related: yes
Cross-species summary: The neuronal ceroid lipofuscinoses (NCLs) are a heterogenous group of inherited neurodegenerative diseases characterised by brain and retinal atrophy and the accumulation of autofluorescent lipopigment in neurons and many other cells within the body. Clinical features of NCL are abnormal behavior, dementia, loss of vision, motor disturbances and seizures, and premature death. See also gene specific entries including OMIA:001504 (PPT1-related), OMIA:001472 (TPP1-related), OMIA:002432 (CLN3-related), OMIA:001482 (CLN5-related), OMIA:001443 (CLN6-related), OMIA:001962 (CLN7/MFSD8-related), OMIA:001506 (CLN8-related), OMIA:001505 (CTSD10-related) and OMIA:001552 (ATP13A2-related).
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Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2026). OMIA:000181-9544: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2026 | Olstad, K., Pastenkos, G., Barrera-Zarate, J., Kanthaswamy, S., Sammak, R., Lemoy, M.J. : |
| Naturally occurring lysosomal storage disease consistent with neuronal ceroid lipofuscinosis in a group of 5 related captive rhesus macaques (Macaca mulatta). Vet Pathol :3009858261445995, 2026. Pubmed reference: 42117273. DOI: 10.1177/03009858261445995. |
Edit History
- Created by Imke Tammen2 on 14 May 2026