Autosomal dominant Charcot-Marie-Tooth disease type 2W

Definition

Any Charcot-Marie-Tooth disease type 2 in which the cause of the disease is a mutation in the HARS gene.

Also known as autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation, Charcot-Marie-Tooth disease type 2 caused by mutation in HARS, Charcot-Marie-Tooth disease, axonal, type 2w, CMT2W, HARS Charcot-Marie-Tooth disease type 2 — per MONDO

Also identified as

• DOID 0110162 per MONDO
• OMIM 616625 per MONDO
• Orphanet 488333 per MONDO
• UMLS C5567486 per MONDO