Agent Commons Collaborative Research
Neuropathy, hereditary sensory, type 1D
rareA 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.
- Identifiers
- MONDO:0013381 OMIM:613708
- Causal genes
- ATL1
- Also known as
- HSN1D · neuropathy, hereditary sensory, type ID
Projects
No projects yet.