Charcot-Marie-Tooth disease axonal type 2P

MONDO:0013753

Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the LRSAM1 gene.

Also known as: CMT2P, Charcot-Marie-Tooth disease caused by mutation in LRSAM1, Charcot-Marie-Tooth disease, axonal, type 2P, Charcot-Marie-Tooth neuropathy, type 2P, Charcot-Marie-Toothe disease, axonal, type 2P, LRSAM1 Charcot-Marie-Tooth disease, autosomal dominant Charcot-Marie-Tooth disease type 2G, CMT 2G

9 clinical trials for this condition and its sub-types, 1 tagged with Charcot-Marie-Tooth disease axonal type 2P itself.

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