Charcot-Marie-Tooth disease type 1C (DOID:0110151)
Alliance: disease page
Synonyms: Charcot-Marie-Tooth neuropathy type 1C; CMT1C; CMT slow nerve conduction type C; HMSN1C; HMSN IC; neuropathy hereditary motor and sensory type 1C
Alt IDs: OMIM:601098, ICD10CM:G60.0, MESH:C537984, ORDO:101083
Definition: A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13.