neuronal ceroid lipofuscinosis 3 (Q32140649)
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A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.
- CLN3
- juvenile neuronal ceroid lipofuscinosis
- Batten disease
- CEROID LIPOFUSCINOSIS, NEURONAL, 3
- Ceroid Lipofuscinosis, Neuronal, type 3
- Spielmeyer-Sjogren Disease
- Vogt-Spielmeyer Disease
- neuronal ceroid lipofuscinosis type 3
- CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3
- Neuronal Ceroid Lipofuscinosis, Juvenile
- CLN3 disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | neuronal ceroid lipofuscinosis 3 |
A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments. |
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C61258
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