DISEASES

Disease-gene associations mined from literature

Human genes for Charcot-Marie-Tooth disease axonal type 2CC

Charcot-Marie-Tooth disease axonal type 2CC [DOID:0110180]

A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NEFH gene on chromosome 22q12.

Synonyms:  Charcot-Marie-Tooth disease axonal type 2CC,  CharcotMarieTooth disease axonal type 2CC,  DOID:0110180,  CMT2CC,  Charcot-Marie-Tooth neuropathy type 2CC ...