Monarch Disease Ontology entry MONDO_0012014 (Charcot-Marie-Tooth disease recessive intermediate A) can be described as follows. Autosomal recessive intermediate Charcot-Marie-Tooth disease type A is a subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by severe, early childhood-onset CMT neuropathy with prominent pes equinovarus deformity and impairment of hand muscles. Nerve conduction velocities usually range between 25-35 m/s and both axonal and demyelinating changes are observed on peripheral nerve pathology. Also known as: CMTRIA, Charcot-Marie-Tooth disease caused by mutation in GDAP1, Charcot-Marie-Tooth disease recessive intermediate type A, Charcot-Marie-Tooth disease, recessive Intermediate type a, Charcot-Marie-Tooth neuropathy recessive intermediate A, GDAP1 Charcot-Marie-Tooth disease, RI-CMT type A, RI-CMTA.