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Boli A-Z Ablepharon-Macrostomia Syndrome Achondrogenesis Achondrogenesis, Type Ii Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aniridia 1 Ankylosis Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autosomal Recessive Stickler Syndrome Back Pain Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Bone Deterioration Disease Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Campomelic Dysplasia Capillary Hemangioma Cataract Chorioretinitis Coffin-Lowry Syndrome Cole Disease Craniosynostosis with Fibular Aplasia Enchondromatosis, Multiple, Ollier Type Epilepsy Fanconi Anemia, Complementation Group E Fibrochondrogenesis Helix Syndrome Hemangioma Hepatic Adenomas, Familial Intervertebral Disc Disease Isolated Pierre Robin Sequence Johanson-Blizzard Syndrome Kniest Dysplasia Macroglossia Marshall Syndrome Multiple Epiphyseal Dysplasia Multiple Epiphyseal Dysplasia Due to Collagen 9 Anomaly Myopia Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondritis Dissecans Otospondylomegaepiphyseal Dysplasia Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive Pierre Robin Syndrome Protrusio Acetabuli Pseudoachondroplasia Renal Glucosuria Retinal Degeneration Retinal Detachment Retinal Perforation Retinitis Scheuermann Disease Spinal Stenosis Stickler Syndrome, Type I Stickler Syndrome, Type Ii Stickler Syndrome, Type Iv Stickler Syndrome, Type V Tetraamelia Syndrome, Autosomal Recessive Uvula, Bifid Vitreoretinal Degeneration Vitreoretinal Dystrophy Vitreous Syneresis Wagner Syndrome