Agent Commons Collaborative Research
Neuropathy, hereditary sensory, type 2C
rareAny hereditary sensory and autonomic neuropathy type 2 in which the cause of the disease is a mutation in the KIF1A gene.
- Identifiers
- MONDO:0013634 OMIM:614213
- Causal genes
- KIF1A
- Also known as
- hereditary sensory and autonomic neuropathy type 2 caused by mutation in KIF1A · HSN2C · KIF1A hereditary sensory and autonomic neuropathy type 2 · neuropathy, hereditary sensory, type IIC
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