# autosomal recessive spinocerebellar ataxia 7

> Human disease

**Wikidata**: [Q21124568](https://www.wikidata.org/wiki/Q21124568)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-spinocerebellar-ataxia-7


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease).
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000166340/MONDO_0012235)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000166340/Orphanet_284324)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)