Home > 2017 ICD-10-CM Diagnosis Codes > Congenital malformations, deformations and chromosomal abnormalities Q00-Q99 > Other congenital malformations Q80-Q89 > Epidermolysis bullosa Q81-
2017 ICD-10-CM Diagnosis Code Q81.9
Epidermolysis bullosa, unspecified
20162017Billable/Specific CodePOA Exempt
Q81.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
This is the American ICD-10-CM version of Q81.9. Other international versions of ICD-10 Q81.9 may differ.
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
A group of chronic skin disorders in which fluid-filled blisters form on the skin and mucosa (the moist, inner lining of some organs and body cavities). Epidermolysis bullosa is inherited and usually starts at birth. Patients with epidermolysis bullosa may be at increased risk of squamous cell cancer of the skin.
An autosomal recessive inherited skin disorder caused by mutations in the genes encoding keratins 5 and 14, collagen vii or laminin 5. It is characterized by skin fragility and the formation of blisters. The blisters may become large and ulcerated, resulting in skin infections and loss of body fluids.
Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties.
Inherited chronic noninflammatory skin disease manifested by vesicles, large bullae (blisters), and skin erosions which often result from trauma.
Present On Admission
Q81.9 is considered exempt from POA reporting.
ICD-10-CM Q81.9 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0):