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.

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  • Created by Imke Tammen2 on 14 May 2026