# autosomal dominant cerebellar ataxia, deafness and narcolepsy

> Human disease

**Wikidata**: [Q21097765](https://www.wikidata.org/wiki/Q21097765)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Autosomal_dominant_cerebellar_ataxia,_deafness,_and_narcolepsy)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-cerebellar-ataxia-deafness-and-narcolepsy


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/6235)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGCIEX:assertion_6235)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000130816/MONDO_0011397)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)
9. UMLS 2023