Term Name: Charcot-Marie-Tooth disease type 1C
Synonyms: Charcot-Marie-Tooth neuropathy type 1C, CMT slow nerve conduction type C, CMT1C, HMSN IC, HMSN1C, neuropathy hereditary motor and sensory type 1C
Definition: A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13.
Ontology: Human Disease [DOID:0110151]   ( DOID:0110151 )

Relationships
is a type of: autosomal dominant disease Charcot-Marie-Tooth disease type 1