# hereditary sensory and autonomic neuropathy type 1C

> hereditary sensory and autonomic neuropathy type 1 that has material basis in heterozygous mutation in the SPTLC2 gene on chromosome 14q24

**Wikidata**: [Q50349723](https://www.wikidata.org/wiki/Q50349723)  
**Source**: https://4ort.xyz/entity/hereditary-sensory-and-autonomic-neuropathy-type-1c


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)