has material basis in autosomal recessive disease Ehlers-Danlos syndrome classic-like 2 MIM:618000 disease_ontology DOID:0080732 An Ehlers-Danlos syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the AEBP1 gene on chromosome 7p13 and that is characterized by severe joint and skin laxity, osteoporosis involving the hips and spine, osteoarthritis, soft redundant skin that can be acrogeria-like, delayed wound healing with abnormal atrophic scarring, and shoulder, hip, knee, and ankle dislocations. Ehlers-Danlos syndrome autosomal recessive inheritance