Term Name:	Charcot-Marie-Tooth disease axonal type 2L
Synonyms:	autosomal dominant axonal Charcot-Marie-Tooth disease type 2L, autosomal dominant Charcot-Marie-Tooth disease type 2L, Charcot-Marie-Tooth neuropathy axonal type 2L, CMT2L
Definition:	A Charcot-Marie-Tooth disease type 2 that has_material_basis_in mutation in the HSPB8 gene.
Ontology:	Human Disease [DOID:0110174]   ( DOID:0110174 )