Q81.1
BillableEpidermolysis bullosa letalis
Epidermolysis bullosa letalis
Status
Billable / Specific
Parent Code
Q81Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Herlitz' syndrome
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
- Generalised junctional epidermolysis bullosa254194001
- Generalized junctional epidermolysis bullosa254194001
- Epidermolysis bullosa letalis400140006
- Herlitz syndrome400140006
- Herlitz's disease400140006
- Junctional epidermolysis bullosa gravis of Herlitz400140006
- Junctional epidermolysis bullosa, lethal type, Herlitz400140006
UMLS
- Bullosa Letali, EpidermolysisC0079683
- Bullosa Letalis, EpidermolysisC0079683
- Bullosa, Herlitz-Pearson-Type EpidermolysisC0079683
- Disease, HerlitzC0079683
- Disease, Herlitz'sC0079683
- EPIDERMOLYSIS BULLOSA JUNCTIONALIS, HERLITZ TYPEC0079683
- EPIDERMOLYSIS BULLOSA LETALISC0079683
- EPIDERMOLYSIS BULLOSA, JUNCTIONAL 1B, SEVEREC0079683
- EPIDERMOLYSIS BULLOSA, JUNCTIONAL, GENERALIZED SEVEREC0079683
- EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPEC0079683
- EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ-PEARSON TYPEC0079683
- Epidermolysis Bullosa Junctionalis, Herlitz TypeC0079683
- Epidermolysis Bullosa LetaliC0079683
- Epidermolysis Bullosa LetalisC0079683
- Epidermolysis Bullosa, Herlitz-Pearson-TypeC0079683
- Epidermolysis Bullosa, Junctional, Herlitz TypeC0079683
- Epidermolysis Bullosa, Junctional, Herlitz-Pearson TypeC0079683
- Epidermolysis bullosa hereditaria letalisC0079683
- Epidermolysis bullosa letalisC0079683
- Epidermolysis bullosa, junctional Herlitz-Pearson typeC0079683
- HERLITZ DISC0079683
- HERLITZ-PEARSON-TYPE EPIDERMOLYSIS BULLOSAC0079683
- HERLITZS DISC0079683
- Herlitz DiseaseC0079683
- Herlitz Pearson Type Epidermolysis BullosaC0079683
- Herlitz syndromeC0079683
- Herlitz' syndromeC0079683
- Herlitz's DiseaseC0079683
- Herlitz's diseaseC0079683
- Herlitz-Pearson Type Epidermolysis BullosaC0079683
- Herlitz-Pearson-Type Epidermolysis BullosaC0079683
- Herlitzs DiseaseC0079683
- JEB-HERLITZ TYPEC0079683
- JEB1BC0079683
- Junctional epidermolysis bullosa gravis of HerlitzC0079683
- Junctional epidermolysis bullosa gravis of Herlitz (disorder)C0079683
- Junctional epidermolysis bullosa, lethal type, HerlitzC0079683
- Letali, Epidermolysis BullosaC0079683
- Letalis, Epidermolysis BullosaC0079683
- Lethal Junctional Epidermolysis BullosaC0079683
Frequently Asked Questions
What is the ICD-10 code for epidermolysis bullosa letalis?
The ICD-10-CM code for epidermolysis bullosa letalis is Q81.1. The full clinical description is "Epidermolysis bullosa letalis". Q81.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q81.1 mean?
ICD-10-CM code Q81.1 represents "Epidermolysis bullosa letalis". 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 Q81.1 a billable code?
Yes, Q81.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q81.1 in?
Q81.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q81.1 map to?
Q81.1 maps to 2 SNOMED CT concepts: 400140006, 254194001. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q81.1?
Q81.1 is linked to 1 UMLS Concept Unique Identifier: C0079683. 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.