has material basis in autosomal recessive disease Ehlers-Danlos syndrome musculocontractural type 1 MIM:601776 DOID:0080736 disease_ontology An Ehlers-Danlos syndrome that is characterized by distinctive craniofacial dysmorphism, congenital contractures of thumbs and fingers, clubfeet, severe kyphoscoliosis, muscular hypotonia, hyperextensible thin skin with easy bruisability and atrophic scarring, wrinkled palms, joint hypermobility, and ocular involvement and that has_material_basis_in homozygous or compound heterozygous mutation in the CHST14 gene on chromosome 15q14. Ehlers-Danlos syndrome autosomal recessive inheritance