Ehlers-Danlos syndrome, musculocontractural type is a congenital form of Ehlers-Danlos syndrome characterized by distinct craniofacial features, multiple contractures, progressive joint and skin laxity, adduction-flexion contractures of the thumbs, talipes equinovarus, bruisability and multisystem fragility-related manifestations. The disease is MONDO_0011142 (Ehlers-Danlos syndrome, musculocontractural type). Also known as: ATCS, CHST14-related EDS, CHST14-related Ehlers-Danlos syndrome, D4ST1-deficient EDS, D4ST1-deficient Ehlers-Danlos syndrome, EDS, Kosho type, EDS, arthrogryposic type, EDS, musculocontractural type.