Charcot-Marie-Tooth disease X-linked recessive 3 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/charcot_marie_tooth_disease_x_linked_recessive_3_2 SCTID:763458005 MEDGEN:375530 CMTX 3 MESH:C535303 DOID:0110211 Orphanet:101077 Charcot-Marie-Tooth neuropathy, X-linked recessive, 3, X-linked recessive UMLS:C1844865 MONDO:0010551 X-linked Charcot-Marie-Tooth disease type 3 is a rare, genetic, peripheral sensorimotor neuropathy characterized by an X-linked recessive inheritance pattern and the childhood- to adolescent-onset of progressive, distal muscle weakness and atrophy (beginning in the lower extremities and then affecting the upper extremities), as well as distal, pansensory loss in the upper and lower extremities, pes cavus, and absent or reduced distal tendon reflexes. Pain and paresthesia are frequently the initial sensory symptoms. Spastic paraparesis (manifested by clasp-knife sign, hyperactive deep-tendon reflexes, and Babinski sign) has also been reported. CMTX3 X-linked Charcot-Marie-Tooth disease type 3 CMT3X Charcot Marie Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease, X-linked recessive, 3 Charcot-Marie-Tooth disease X-linked recessive type 3 GARD:0001244 OMIM:302802 Charcot-Marie-Tooth neuropathy, X-linked recessive, 3 Charcot-Marie-Tooth disease type X