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Summary Literature (0)
OMIM:616625 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W; CMT2W


Xenbase Genes: hars1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014711 - autosomal dominant Charcot-Marie-Tooth disease type 2W