Diagnosis Code: Q81.2

Short Description: Epidermolysis bullosa dystrophica

Long Description: Epidermolysis bullosa dystrophica

The code Q81.2 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Other congenital malformations (Q80-Q89)
    • Epidermolysis bullosa (Q81)
      • Q81.2 Epidermolysis bullosa dystrophica

Code Version: 2022 ICD-10-CM

Synonyms

• Acral dystrophic epidermolysis bullosa
• Autosomal dominant generalized dystrophic epidermolysis bullosa
• Centripetalis recessive dystrophic epidermolysis bullosa
• Dominant dystrophic epidermolysis bullosa
• Dominant dystrophic epidermolysis bullosa with absence of skin
• Dominant dystrophic epidermolysis bullosa, albopapular type
• Dystrophic epidermolysis bullosa
• Dystrophic epidermolysis bullosa inverse type
• Dystrophic epidermolysis bullosa nails only
• Generalized dystrophic epidermolysis bullosa
• Generalized recessive dystrophic epidermolysis bullosa mitis
• Generalized recessive non-mutilating dystrophic epidermolysis bullosa
• Localized dystrophic epidermolysis bullosa
• Localized recessive dystrophic epidermolysis bullosa
• Progressive recessive dystrophic epidermolysis bullosa
• Recessive dystrophic epidermolysis bullosa
• Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type
• Severe generalized recessive dystrophic epidermolysis bullosa

Diagnostic Related Group(s)

The code Q81.2 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Minor Skin Disorders With Mcc (606)
• Minor Skin Disorders Without Mcc (607)

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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