ICD-10 Diagnosis Code Q81.8

Other epidermolysis bullosa

Diagnosis Code Q81.8

ICD-10: Q81.8
Short Description: Other epidermolysis bullosa
Long Description: Other epidermolysis bullosa
This is the 2018 version of the ICD-10-CM diagnosis code Q81.8

Valid for Submission
The code Q81.8 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Other congenital malformations (Q80-Q89)
      • Epidermolysis bullosa (Q81)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code Q81.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG V34.0)


Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

Present on Admission (POA) Additional informationCallout TooltipPresent on Admission
The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement.

The code Q81.8 is exempt from POA reporting.

  • Aplasia cutis congenita in association with epidermolysis bullosa
  • Cicatricial junctional epidermolysis bullosa
  • Congenital junctional epidermolysis bullosa
  • Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
  • Dominant epidermolysis bullosa simplex, Weber-Cockayne type
  • Epidermolysis bullosa pruriginosa
  • Gastric atresia
  • Generalized dystrophic epidermolysis bullosa
  • Generalized junctional epidermolysis bullosa
  • Inverse junctional epidermolysis bullosa
  • Junctional epidermolysis bullosa
  • Junctional epidermolysis bullosa mitis
  • Localized junctional epidermolysis bullosa
  • Progressive junctional epidermolysis bullosa
  • Pyloric atresia

Information for Patients

Skin Conditions

Also called: Cutaneous disorders, Dermatologic disorders

Your skin is your body's largest organ. It covers and protects your body. Your skin

  • Holds body fluids in, preventing dehydration
  • Keeps harmful microbes out, preventing infections
  • Helps you feel things like heat, cold, and pain
  • Keeps your body temperature even
  • Makes vitamin D when the sun shines on it

Anything that irritates, clogs, or inflames your skin can cause symptoms such as redness, swelling, burning, and itching. Allergies, irritants, your genetic makeup, and certain diseases and immune system problems can cause rashes, hives, and other skin conditions. Many skin problems, such as acne, also affect your appearance.

NIH: National Institute of Arthritis and Musculoskeletal and Skin Diseases

  • Acrodermatitis (Medical Encyclopedia)
  • Cryotherapy (Medical Encyclopedia)
  • Cutaneous skin tags (Medical Encyclopedia)
  • Dry skin -- self-care (Medical Encyclopedia)
  • Erythema multiforme (Medical Encyclopedia)
  • Granuloma annulare (Medical Encyclopedia)
  • Keratosis pilaris (Medical Encyclopedia)
  • Lichen planus (Medical Encyclopedia)
  • Milia (Medical Encyclopedia)
  • Sebaceous cyst (Medical Encyclopedia)
  • Seborrheic keratosis (Medical Encyclopedia)
  • Skin lesion removal (Medical Encyclopedia)
  • Skin lesion removal-aftercare (Medical Encyclopedia)
  • Stasis dermatitis and ulcers (Medical Encyclopedia)

[Read More]

Junctional epidermolysis bullosa Junctional epidermolysis bullosa (JEB) is one of the major forms of epidermolysis bullosa, a group of genetic conditions that cause the skin to be very fragile and to blister easily. Blisters and skin erosions form in response to minor injury or friction, such as rubbing or scratching. Researchers classify junctional epidermolysis bullosa into two main types: Herlitz JEB and non-Herlitz JEB. Although the types differ in severity, their features overlap significantly, and they can be caused by mutations in the same genes.Herlitz JEB is the more severe form of the condition. From birth or early infancy, affected individuals have blistering over large regions of the body. Blistering also affects the mucous membranes, such as the moist lining of the mouth and digestive tract, which can make it difficult to eat and digest food. As a result, many affected children have chronic malnutrition and slow growth. The extensive blistering leads to scarring and the formation of red, bumpy patches called granulation tissue. Granulation tissue bleeds easily and profusely, making affected infants susceptible to serious infections and loss of necessary proteins, minerals, and fluids. Additionally, a buildup of granulation tissue in the airway can lead to a weak, hoarse cry and difficulty breathing.Other complications of Herlitz JEB can include fusion of the fingers and toes, abnormalities of the fingernails and toenails, joint deformities (contractures) that restrict movement, and hair loss (alopecia). Because the signs and symptoms of Herlitz JEB are so severe, infants with this condition usually do not survive beyond the first year of life.The milder form of junctional epidermolysis bullosa is called non-Herlitz JEB. The blistering associated with non-Herlitz JEB may be limited to the hands, feet, knees, and elbows, and it often improves after the newborn period. Other characteristic features of this condition include alopecia, malformed fingernails and toenails, and irregular tooth enamel. Most affected individuals do not have extensive scarring or granulation tissue formation, so breathing difficulties and other severe complications are rare. Non-Herlitz JEB is typically associated with a normal lifespan.
[Read More]
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