Charcot-Marie-Tooth disease X-linked recessive 2 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/charcot_marie_tooth_disease_x_linked_recessive_2_2 SCTID:763457000 X-linked Charcot-Marie-Tooth disease type 2 GARD:0001243 Charcot-Marie-Tooth disease X-linked recessive type 2 Charcot Marie Tooth disease X-linked recessive 2 DOID:0110208 OMIM:302801 Charcot-Marie-Tooth neuropathy, X-linked recessive, 2 UMLS:C1844873 CMTX 2 MESH:C535302 Charcot-Marie-Tooth neuropathy, X-linked recessive, 2, X-linked recessive Orphanet:101076 Charcot-Marie-Tooth disease, X-linked recessive, 2 X-linked Charcot-Marie-Tooth disease type 2 is a rare, genetic, peripheral sensorimotor neuropathy characterized by an X-linked recessive inheritance pattern and the infantile- to childhood-onset of progressive, distal muscle weakness and atrophy (more prominent in the lower extremities than in the upper extremities), pes cavus, and absent tendon reflexes. Sensory impairment and intellectual disability has been reported in some individuals. MEDGEN:336803 CMTX2 MONDO:0010550 Charcot-Marie-Tooth disease type X