Human genes for Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease type 1B [DOID:0110152]
A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the gene encoding myelin protein zero (MPZ).
Synonyms: Charcot-Marie-Tooth disease type 1B, CharcotMarieTooth disease type 1B, DOID:0110152, autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B, Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy ...