ICD-9-CM 756.83 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 756.83 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
A heterogeneous group of autosomally inherited collagen diseases caused by defects in the synthesis or structure of fibrillar collagen. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability
An inherited connective tissue disorder characterized by loose and fragile skin and joint hypermobility
Ehlers-danlos syndrome (eds) is a group of inherited disorders that weaken connective tissues. Connective tissues are proteins that support skin, bones, blood vessels and other organs. Eds usually affects your skin, joints and blood vessel walls. Symptoms include
loose joints
fragile, small blood vessels
abnormal scar formation and wound healing
soft, velvety, stretchy skin that bruises easily
there are several types of eds. They can range from mild to life-threatening. About 1 in 5,000 people has eds. There is no cure. Treatment involves managing symptoms. It also includes learning how to protect your joints and prevent injuries
Group of inherited disorders of the connective tissue; major manifestations include hyperextensible skin and joints, easy bruisability, friability of tissues with bleeding and poor wound healing, calcified subcutaneous spheroids, and pseudotumors