AutoICD API

Q81.2

Billable

Epidermolysis bullosa dystrophica

Epidermolysis bullosa dystrophica

Status

Billable / Specific

Parent Code

Q81

ICD-11 Mapping

1 equivalent

Coding Notes

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(4)
Q81.0

Epidermolysis bullosa simplex

BillableQ81.1

Epidermolysis bullosa letalis

BillableQ81.8

Other epidermolysis bullosa

BillableQ81.9

Epidermolysis bullosa, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

EC32Dystrophic epidermolysis bullosaequivalentPrimary
Also Known As / Clinical Terms(144)

SNOMED CT

UMLS

Clinical Terms

  • Dystrophic epidermolysis bullosa
  • DEB
  • Dominant dystrophic epidermolysis bullosa with absence of skin
  • Generalized dystrophic epidermolysis bullosa
  • Epidermolysis bullosa, dystrophic
  • Localized dystrophic epidermolysis bullosa
  • bullosa dystrophic epidermolysis
  • Nails only DEB (dystrophic epidermolysis bullosa)
  • Generalised recessive non-mutilating dystrophic epidermolysis bullosa
  • Acral dystrophic epidermolysis bullosa
  • Dominant dystrophic epidermolysis bullosa of Pasini
  • Autosomal recessive dystrophic epidermolysis bullosa generalisata gravis
  • Generalised dystrophic epidermolysis bullosa
  • Generalized DDEB (generalized dystrophic epidermolysis bullosa)
  • Bullosa Dystrophica, Epidermolysis
  • Dystrophic epidermolysis bullosa inverse type
  • Bullosa, Dystrophic Epidermolysis
  • Albopapuloid dystrophic epidermolysis bullosa of Pasini
  • Autosomal dominant generalised dystrophic epidermolysis bullosa
  • Dominant dystrophic epidermolysis bullosa, albopapular type
  • Goldscheider's disease
  • Localised dystrophic epidermolysis bullosa
  • RDEB-O - recessive dystrophic epidermolysis bullosa-generalized other
  • Dystrophic epidermolysis bullosa (disorder)
  • Dystrophic epidermolysis bullosa nails only
  • Recessive dystrophic epidermolysis bullosa
  • Generalized recessive non-mutilating dystrophic epidermolysis bullosa
  • Epidermolysis bullosa dystrophica, Pasini type
  • RDEB-O - recessive dystrophic epidermolysis bullosa-generalised other
  • Centripetal recessive dystrophic epidermolysis bullosa
  • Bullosa Dystrophicas, Epidermolysis
  • epidermolysis bullosa dystrophic
  • Polydysplastic epidermolysis bullosa
  • Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type
  • Dystrophicas, Epidermolysis Bullosa
  • Generalised recessive dystrophic epidermolysis bullosa mitis
  • Hyperplastic epidermolysis bullosa
  • Bullosas, Dystrophic Epidermolysis
  • Goldscheider disease
  • DDEB (dominant dystrophic epidermolysis bullosa) intermediate
  • Dysplastic epidermolysis bullosa dystrophica
  • Localised recessive dystrophic epidermolysis bullosa
  • Severe generalised recessive dystrophic epidermolysis bullosa
  • bullosa dystrophica epidermolysis
  • Epidermolysis Bullosas, Dystrophic
  • Centripetalis recessive dystrophic epidermolysis bullosa
  • Dominant dystrophic epidermolysis bullosa
  • Progressive recessive dystrophic epidermolysis bullosa
  • Epidermolysis Bullosa Dystrophicas
  • Epidermolysis bullosa dystrophica, Bart type
  • DEB - Dystrophic epidermolysis bullosa
  • Autosomal recessive dystrophic epidermolysis bullosa Hallopeau Siemens type
  • Epidermolysis bullosa dystrophica dominans
  • RDEB-Ce - recessive dystrophic epidermolysis bullosa centripetalis
  • Dystrophic Epidermolysis Bullosas
  • Cockayne Touraine epidermolysis bullosa
  • Autosomal dominant generalized dystrophic epidermolysis bullosa
  • EBR 3
  • Localized recessive dystrophic epidermolysis bullosa
  • Severe generalized recessive dystrophic epidermolysis bullosa
  • Epidermolysis bullosa dystrophica neurotrophica
  • Hyperplastic dystrophic epidermolysis bullosa
  • Generalized recessive dystrophic epidermolysis bullosa mitis
  • Dystrophica, Epidermolysis Bullosa
  • Dystrophic epidermolysis bullosa generalisata mitis
  • Generalised DDEB (generalised dystrophic epidermolysis bullosa)
  • Acral DEB (dystrophic epidermolysis bullosa)
  • Epidermolysis bullosa, Cockayne-Touraine type
Frequently Asked Questions
What is the ICD-10 code for epidermolysis bullosa dystrophica?

The ICD-10-CM code for epidermolysis bullosa dystrophica is Q81.2. The full clinical description is "Epidermolysis bullosa dystrophica". Q81.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q81.2 mean?

ICD-10-CM code Q81.2 represents “Epidermolysis bullosa dystrophica”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q81.2 a billable code?

Yes, Q81.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q81.2 in?

Q81.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q81.2 map to?

Q81.2 maps to 18 SNOMED CT concepts: 733638006, 75875004, 1231284001, 723716009, 725419003, and 13 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q81.2?

Q81.2 is linked to 1 UMLS Concept Unique Identifier: C0079294. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q81.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like epidermolysis bullosa dystrophica affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q81.2?

Q81.2 maps to the ICD-11 code: EC32 (Dystrophic epidermolysis bullosa).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.