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DO Term : Charcot-Marie-Tooth disease, axonal type 2W [DOID:0110162] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the HARS gene on chromosome 5q31.
  • synonyms:
  • autosomal dominant axonal Charcot-Marie-Tooth disease type 2W,
  • 616625,
  • CMT2W,
  • Charcot-Marie-Tooth neuropathy type 2W,
  • OMIM:616625
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