Q81.8
BillableOther epidermolysis bullosa
Other epidermolysis bullosa
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(115)
SNOMED CT
- Pyloric atresia27729002
- Atresia of stomach28828001
- Atretogastria28828001
- Gastric atresia28828001
- Imperforate stomach28828001
- Abnormal granulation tissue31825002
- Excessive granulation tissue31825002
- Exuberant granulation tissue31825002
- Proud flesh31825002
- Congenital junctional epidermolysis bullosa-pyloric atresia syndrome53748002
- Epidermolysis bullosa letalis with pyloric atresia53748002
- Congenital junctional epidermolysis bullosa79855003
- Epidermolysis bullosa hereditaria letalis79855003
- Epidermolysis bullosa, junctional Herlitz-Pearson type79855003
- Generalised dystrophic epidermolysis bullosa254188009
- Generalized dystrophic epidermolysis bullosa254188009
- Localised junctional epidermolysis bullosa254191009
- Localized junctional epidermolysis bullosa254191009
- Epidermolysis atrophicans inversa254192002
- Inverse junctional epidermolysis bullosa254192002
- Epidermolysis bullosa progressiva254193007
- Junctional epidermolysis bullosa progressiva254193007
- Progressive junctional epidermolysis bullosa (neurotrophic)254193007
- Generalised junctional epidermolysis bullosa254194001
- Generalized junctional epidermolysis bullosa254194001
- Generalised atrophic benign epidermolysis bullosa - GABEB254196004
- Generalised junctional epidermolysis bullosa non-Herlitz type254196004
- Generalized atrophic benign epidermolysis bullosa - GABEB254196004
- Generalized junctional epidermolysis bullosa non-Herlitz type254196004
- Junctional epidermolysis bullosa Disentis type254196004
- Junctional epidermolysis bullosa generalised intermediate254196004
- Junctional epidermolysis bullosa generalized intermediate254196004
- Junctional epidermolysis bullosa mitis254196004
- Cicatricial junctional epidermolysis bullosa254197008
- DEBS-WC294705005
- Dominant epidermolysis bullosa simplex, Weber-Cockayne type294705005
- Epidermolysis bullosa simplex of the hands AND/OR feet294705005
- Weber-Cockayne syndrome294705005
- Granulation of skin297959007
- Autosomal dominant epidermolysis bullosa simplex398170002
- EBS 1398170002
- Junctional epidermolysis bullosa399971009
- Aplasia cutis congenita in association with epidermolysis bullosa (Type 6)403550004
- Epidermolysis bullosa pruriginosa403810008
- Late-onset junctional epidermolysis bullosa719432000
- LOC syndrome722675000
- LOGIC syndrome722675000
- Laryngo-onycho-cutaneous syndrome722675000
- Laryngoonychocutaneous syndrome722675000
- Shabbir syndrome722675000
- Junctional epidermolysis bullosa non-Herlitz type724225008
- Late-onset localised junctional epidermolysis bullosa, intellectual disability syndrome773692000
- Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome773692000
- Localised junctional epidermolysis bullosa non-Herlitz type1254890002
- Localised non-Herlitz junctional epidermolysis bullosa1254890002
- Localized junctional epidermolysis bullosa non-Herlitz type1254890002
- Localized non-Herlitz junctional epidermolysis bullosa1254890002
Clinical Terms
- LOC syndrome
- Junctional epidermolysis bullosa
- Proud flesh
- Excessive granulation tissue
- Generalized dystrophic epidermolysis bullosa
- Epidermolysis bullosa hereditaria letalis
- Generalised junctional epidermolysis bullosa
- Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
- Abnormal granulation tissue
- Imperforate stomach
- Junctional epidermolysis bullosa generalized intermediate
- Dominant epidermolysis bullosa simplex, Weber-Cockayne type
- Generalised dystrophic epidermolysis bullosa
- Epidermolysis bullosa pruriginosa
- Generalised junctional epidermolysis bullosa non-Herlitz type
- LOGIC syndrome
- Atresia of stomach
- Localized non-Herlitz junctional epidermolysis bullosa
- Pyloric atresia
- Aplasia cutis congenita in association with epidermolysis bullosa (Type 6)
- Epidermolysis bullosa simplex of the hands AND/OR feet
- Junctional epidermolysis bullosa non-Herlitz type
- Epidermolysis bullosa, junctional Herlitz-Pearson type
- Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome
- Atretogastria
- Junctional epidermolysis bullosa Disentis type
- Epidermolysis bullosa progressiva
- Late-onset localised junctional epidermolysis bullosa, intellectual disability syndrome
- Progressive junctional epidermolysis bullosa (neurotrophic)
- Generalized junctional epidermolysis bullosa
- Granulation of skin
- Cicatricial junctional epidermolysis bullosa
- DEBS-WC
- Gastric atresia
- Generalised atrophic benign epidermolysis bullosa - GABEB
- Localised junctional epidermolysis bullosa
- Congenital junctional epidermolysis bullosa
- Epidermolysis bullosa letalis with pyloric atresia
- Inverse junctional epidermolysis bullosa
- Junctional epidermolysis bullosa progressiva
- Autosomal dominant epidermolysis bullosa simplex
- Laryngo-onycho-cutaneous syndrome
- Localised junctional epidermolysis bullosa non-Herlitz type
- Generalized atrophic benign epidermolysis bullosa - GABEB
- Junctional epidermolysis bullosa generalised intermediate
- Junctional epidermolysis bullosa mitis
- Late-onset junctional epidermolysis bullosa
- Laryngoonychocutaneous syndrome
- Localised non-Herlitz junctional epidermolysis bullosa
- EBS 1
- Exuberant granulation tissue
- Generalized junctional epidermolysis bullosa non-Herlitz type
- Shabbir syndrome
- Weber-Cockayne syndrome
- Epidermolysis atrophicans inversa
- Localized junctional epidermolysis bullosa non-Herlitz type
- Localized junctional epidermolysis bullosa
Frequently Asked Questions
What is the ICD-10 code for other epidermolysis bullosa?
The ICD-10-CM code for other epidermolysis bullosa is Q81.8. The full clinical description is "Other epidermolysis bullosa". Q81.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q81.8 mean?
ICD-10-CM code Q81.8 represents “Other epidermolysis bullosa”. 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 Q81.8 a billable code?
Yes, Q81.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q81.8 in?
Q81.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q81.8 map to?
Q81.8 maps to 23 SNOMED CT concepts: 31825002, 403550004, 28828001, 398170002, 254197008, and 18 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q81.8?
Q81.8 is linked to 1 UMLS Concept Unique Identifier: C0478085. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q81.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other epidermolysis bullosa 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 Q81.8?
Q81.8 maps to the ICD-11 code: EC3Z (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.