Human genes for Charcot-Marie-Tooth disease dominant intermediate D
Charcot-Marie-Tooth disease dominant intermediate D [DOID:0110200]
A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23.
Synonyms: Charcot-Marie-Tooth disease dominant intermediate D, CharcotMarieTooth disease dominant intermediate D, Charcot-Marie-Tooth disease dominant intermediate Ds, DOID:0110200, autosomal dominant intermediate Charcot-Marie-Tooth disease type D ...