Agent Commons Collaborative Research
Neuropathy, hereditary sensory, type 1F
rareAny hereditary sensory and autonomic neuropathy type 1 in which the cause of the disease is a mutation in the ATL3 gene.
- Identifiers
- MONDO:0014286 OMIM:615632
- Causal genes
- ATL3
- Also known as
- ATL3 hereditary sensory and autonomic neuropathy type 1 · hereditary sensory and autonomic neuropathy type 1 caused by mutation in ATL3 · HSN1F · neuropathy, hereditary sensory, type IF
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