Q81.2
BillableEpidermolysis bullosa dystrophica
Epidermolysis bullosa dystrophica
Status
Billable / Specific
Parent Code
Q81Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Dominant dystrophic epidermolysis bullosa with absence of skin2689001
- Epidermolysis bullosa dystrophica, Bart type2689001
- Dysplastic epidermolysis bullosa dystrophica48528004
- Polydysplastic epidermolysis bullosa48528004
- Recessive dystrophic epidermolysis bullosa48528004
- Albopapuloid dystrophic epidermolysis bullosa of Pasini75875004
- Dominant dystrophic epidermolysis bullosa of Pasini75875004
- Dominant dystrophic epidermolysis bullosa, albopapular type75875004
- Epidermolysis bullosa dystrophica, Pasini type75875004
- Cockayne Touraine epidermolysis bullosa111389006
- Dominant dystrophic epidermolysis bullosa111389006
- Epidermolysis bullosa dystrophica dominans111389006
- Epidermolysis bullosa, Cockayne-Touraine type111389006
- Hyperplastic dystrophic epidermolysis bullosa111389006
- Hyperplastic epidermolysis bullosa111389006
- EBR 3254176007
- Epidermolysis bullosa dystrophica neurotrophica254176007
- Goldscheider disease254176007
- Goldscheider's disease254176007
- Progressive recessive dystrophic epidermolysis bullosa254176007
- DEB - Dystrophic epidermolysis bullosa254185007
- Dystrophic epidermolysis bullosa254185007
- Epidermolysis bullosa dystrophica254185007
- Localised dystrophic epidermolysis bullosa254186008
- Localized dystrophic epidermolysis bullosa254186008
- Localised recessive dystrophic epidermolysis bullosa254187004
- Localized recessive dystrophic epidermolysis bullosa254187004
- Generalised dystrophic epidermolysis bullosa254188009
- Generalized dystrophic epidermolysis bullosa254188009
- Generalised recessive dystrophic epidermolysis bullosa mitis254189001
- Generalized recessive dystrophic epidermolysis bullosa mitis254189001
- Dystrophic epidermolysis bullosa generalisata mitis403808006
- Generalised recessive non-mutilating dystrophic epidermolysis bullosa403808006
- Generalized recessive non-mutilating dystrophic epidermolysis bullosa403808006
- Dystrophic epidermolysis bullosa inverse type403809003
- Dystrophic epidermolysis bullosa nails only722436002
- Nails only DEB (dystrophic epidermolysis bullosa)722436002
- Autosomal recessive dystrophic epidermolysis bullosa Hallopeau Siemens type723716009
- Autosomal recessive dystrophic epidermolysis bullosa generalisata gravis723716009
- Severe generalised recessive dystrophic epidermolysis bullosa723716009
- Severe generalized recessive dystrophic epidermolysis bullosa723716009
- RDEB-O - recessive dystrophic epidermolysis bullosa-generalised other725407006
- RDEB-O - recessive dystrophic epidermolysis bullosa-generalized other725407006
- Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type725407006
- Centripetal recessive dystrophic epidermolysis bullosa725419003
- Centripetalis recessive dystrophic epidermolysis bullosa725419003
- RDEB-Ce - recessive dystrophic epidermolysis bullosa centripetalis725419003
- Acral DEB (dystrophic epidermolysis bullosa)733638006
- Acral dystrophic epidermolysis bullosa733638006
- Autosomal dominant generalised dystrophic epidermolysis bullosa1231284001
- Autosomal dominant generalized dystrophic epidermolysis bullosa1231284001
- DDEB (dominant dystrophic epidermolysis bullosa) intermediate1231284001
- Generalised DDEB (generalised dystrophic epidermolysis bullosa)1231284001
- Generalized DDEB (generalized dystrophic epidermolysis bullosa)1231284001
UMLS
- Bullosa Dystrophica, EpidermolysisC0079294
- Bullosa Dystrophicas, EpidermolysisC0079294
- Bullosa, Dystrophic EpidermolysisC0079294
- Bullosas, Dystrophic EpidermolysisC0079294
- DEBC0079294
- DEB - Dystrophic epidermolysis bullosaC0079294
- Dystrophic Epidermolysis BullosaC0079294
- Dystrophic Epidermolysis BullosasC0079294
- Dystrophic epidermolysis bullosaC0079294
- Dystrophic epidermolysis bullosa (disorder)C0079294
- Dystrophica, Epidermolysis BullosaC0079294
- Dystrophicas, Epidermolysis BullosaC0079294
- Epidermolysis Bullosa DystrophicaC0079294
- Epidermolysis Bullosa DystrophicasC0079294
- Epidermolysis Bullosa, DystrophicC0079294
- Epidermolysis Bullosas, DystrophicC0079294
- Epidermolysis bullosa dystrophicaC0079294
- Epidermolysis bullosa, dystrophicC0079294
- bullosa dystrophic epidermolysisC0079294
- bullosa dystrophica epidermolysisC0079294
- dystrophic epidermolysis bullosaC0079294
- epidermolysis bullosa dystrophicC0079294
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.
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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.