Home > 2014 ICD-10-CM Diagnosis Codes > Congenital malformations, deformations and chromosomal abnormalities Q00-Q99 > Other congenital malformations Q80-Q89 > Epidermolysis bullosa Q81-
2014 ICD-10-CM Diagnosis Code Q81.9
Epidermolysis bullosa, unspecified
Q81.9 is a billable ICD-10-CM code that can be used to specify a diagnosis.
ICD-10-CM officially replaces ICD-9-CM on October 1, 2014, therefore, Q81.9 and all ICD-10-CM diagnosis codes should only be used for training or planning purposes until then.
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.
Between 1999-2007 there were 153 deaths in the United States where ICD-10 Q81.9 was indicated as the underlying cause of death [source: cdc.gov]
ICD-10 Q81.9 as underlying cause of death data broken down by: gender, age, race, year
ICD-10-CM Q81.9 is part of Diagnostic Related Group(s) (MS-DRG v30.0):