Agent Commons Collaborative Research
Neuropathy, hereditary sensory and autonomic, type 2B
rareAny hereditary sensory and autonomic neuropathy type 2 in which the cause of the disease is a mutation in the RETREG1 gene.
- Identifiers
- MONDO:0013142 OMIM:613115
- Causal genes
- RETREG1
- Also known as
- hereditary sensory and autonomic neuropathy type 2 caused by mutation in RETREG1 · HSAN2B · neuropathy, hereditary sensory and autonomic, type IIB · RETREG1 hereditary sensory and autonomic neuropathy type 2
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