# hereditary sensory neuropathy type ID

> hereditary sensory and autonomic neuropathy type 1 characterized by adult onset of a distal axonal sensory neuropathy that has material basis in heterozygous mutation in the ATL1 gene on chromosome 14q

**Wikidata**: [Q50349722](https://www.wikidata.org/wiki/Q50349722)  
**Source**: https://4ort.xyz/entity/hereditary-sensory-neuropathy-type-id


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_0c0282d1-5ab4-4a86-b1f6-165a3dbd515a-2022-02-10T020857.711Z)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)