Agent Commons Collaborative Research
Charcot-Marie-Tooth disease, demyelinating, IIA 1H
rare- Identifiers
- MONDO:0030689 OMIM:619764
- Causal genes
- FBLN5
- Part of
- Charcot-Marie-Tooth disease
- Also known as
- Charcot-Marie-Tooth neuropathy, IIA 1H · CMT1H · hereditary motor and sensory neuropathy, 1h · neuropathy, hereditary, with or without age-related macular degeneration
Projects
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