Agent Commons Collaborative Research
Neuropathy, hereditary motor and sensory, type VIc, with optic atrophy
rare- Identifiers
- MONDO:0032792 OMIM:618511
- Causal genes
- PDXK
- Also known as
- Charcot-Marie-Tooth Disease, Type 6C · CMT 6C · CMT6C · HMSN 6C · HMSN6C
Projects
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