DISEASES

Disease-gene associations mined from literature

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Human genes for neuronal ceroid lipofuscinosis 6A

Neuronal ceroid lipofuscinosis 6A [DOID:0110729]

A neuronal ceroid lipofuscinosis that is characterized by progressive decline of neurologic function, including visual deterioration in most, cognitive impairment, loss of motor function, and seizures and has_material_basis_in homozygous mutation in the CLN6 gene on chromosome 15q21-q23.

Synonyms:  neuronal ceroid lipofuscinosis 6A,  DOID:0110729,  neuronal ceroid lipofuscinosis 6,  neuronal ceroid lipofuscinosis 6 variable age of onset

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.