Connective Tissue Disorders

Related topics on Genetics Home Reference:

• achondrogenesis
• Alport syndrome
• arterial tortuosity syndrome
• congenital contractural arachnodactyly
• cutis laxa
• Czech dysplasia
• dystrophic epidermolysis bullosa
• Ehlers-Danlos syndrome
• homocystinuria
• hypochondrogenesis
• juvenile idiopathic arthritis
• Kniest dysplasia
• Loeys-Dietz syndrome
• Marfan syndrome
• mucopolysaccharidosis type I
• mucopolysaccharidosis type II
• mucopolysaccharidosis type III
• mucopolysaccharidosis type IV
• mucopolysaccharidosis type VI
• mucopolysaccharidosis type VII
• Noonan syndrome
• osteogenesis imperfecta
• otospondylomegaepiphyseal dysplasia
• platyspondylic lethal skeletal dysplasia, Torrance type
• pseudoxanthoma elasticum
• Shprintzen-Goldberg syndrome
• spondyloepimetaphyseal dysplasia, Strudwick type
• spondyloepiphyseal dysplasia congenita
• spondyloperipheral dysplasia
• Stickler syndrome
• systemic scleroderma
• Weill-Marchesani syndrome
• Weissenbacher-Zweymüller syndrome

You may also search Genetics Home Reference for "Connective Tissue Disorders" for additional information.