# neuronal ceroid lipofuscinosis 3

> 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

**Wikidata**: [Q32140649](https://www.wikidata.org/wiki/Q32140649)  
**Source**: https://4ort.xyz/entity/neuronal-ceroid-lipofuscinosis-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000188603/MONDO_0008767)
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000188603/Orphanet_228346)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)
7. UMLS 2023