Connective Tissue Disorders
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Aortic valve disease 1
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Arterial tortuosity syndrome
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Bone mineral density QTL18 - osteoporosis
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Brittle cornea syndrome
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Bruck syndrome
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Congenital contractural arachnodactyly
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Cutis laxa - autosomal dominant
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Cutis laxa - autosomal recessive - type IIB
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Cutis laxa autosomal dominant 2
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Cutis laxa autosomal recessive - Cutis laxa type IA
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Cutis laxa autosomal recessive - Cutis laxa type IB
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Cutis laxa autosomal recessive - Cutis laxa type IC
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Ectopia lentis
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Ehlers-Danlos syndrome - EDS
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Ehlers-Danlos syndrome kyphoscoliotic type
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Ehlers-Danlos syndrome type I - classic type
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Ehlers-Danlos syndrome type II - classic type
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Ehlers-Danlos syndrome vascular type
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Ehlers-Danlos syndrome with progressive kyphoscoliosis myopathy and hearing loss
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Geleophysic dysplasia
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Homocystinuria
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Hypophosphatasia
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Kniest dysplasia
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Larsen syndrome
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Loeys-Dietz syndrome type 1A
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Loeys-Dietz syndrome type 1B
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Loeys-Dietz syndrome type 2A
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Loeys-Dietz syndrome type 2B
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Loeys-Dietz syndrome type 3 - aneurysms-osteoarthritis syndrome
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Loeys-Dietz syndrome type 4
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Lysyl hydroxylase 3 deficiency
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Marfan Syndrome
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Marshall syndrome
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Metaphyseal chondrodysplasia Schmid type
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Multiple epiphyseal dysplasia
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Multiple joint dislocations short stature craniofacial dysmorphism and congenital heart defects
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Multiple self-healing squamous epithelioma
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Osteogenesis imperfecta
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Osteogenesis imperfecta type IX
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Osteogenesis imperfecta type V
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Osteogenesis imperfecta type VIII
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Osteogenesis imperfecta type X
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Osteogenesis imperfecta type XII
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Osteoporosis - early onset
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Osteoporosis with fractures
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Osteoporosis-pseudoglioma syndrome
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Otospondylomegaepiphyseal dysplasia
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Porencephaly
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Spondylocheirodysplasia
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Spondyloepiphyseal dysplasia congenita
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Stickler syndrome
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Supravalvular aortic stenosis
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Thoracic Aortic Aneurysm with Dissection - TAAD
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van den Ende-Gupta syndrome
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Wagner syndrome
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Weill-Marchesani syndrome
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Weissenbacher-Zweymuller syndrome