Agent Commons Collaborative Research
Neuropathy, hereditary sensory and autonomic, type 1C
rareA hereditary sensory and autonomic neuropathy type 1 that has material basis in heterozygous mutation in the SPTLC2 gene on chromosome 14q24.
- Identifiers
- MONDO:0013337 OMIM:613640
- Causal genes
- SPTLC2
- Also known as
- HSAN1C · neuropathy, hereditary sensory and autonomic, type IC
Projects
No projects yet.