# hereditary sensory neuropathy-deafness-dementia syndrome

> hereditary sensory neuropathy characterized by adult onset of progressive peripheral sensory loss, progressive hearing impairment, and early-onset dementia that has material basis in heterozygous mutation in the DNMT1 gene on chromosome 19p13

**Wikidata**: [Q50349724](https://www.wikidata.org/wiki/Q50349724)  
**Source**: https://4ort.xyz/entity/hereditary-sensory-neuropathy-deafness-dementia-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000130816/MONDO_0013584)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)