Q81.0
BillableEpidermolysis bullosa simplex
Epidermolysis bullosa simplex
Status
Billable / Specific
Parent Code
Q81Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Pyloric atresia27729002
- Atresia of stomach28828001
- Atretogastria28828001
- Gastric atresia28828001
- Imperforate stomach28828001
- Epidermolysis bullosa simplex67144006
- Epidermolysis bullosa simplex, Kobner type90496008
- Generalised epidermolysis bullosa simplex90496008
- Generalized epidermolysis bullosa simplex90496008
- Kobner disease90496008
- Koebner epidermolysis bullosa90496008
- Epidermolysis bullosa simplex with hypodontia254177003
- Kallin's syndrome254177003
- Dowling-Meara epidermolysis bullosa254179000
- Epidermolysis bullosa simplex herpetiformis254179000
- Simplex epidermolysis bullosa herpetiformis254179000
- Epidermolysis bullosa simplex with mottled pigmentation254180002
- Simple epidermolysis bullosa with mottled pigmentation254180002
- Epidermolysis simplex superficialis254181003
- Lethal autosomal recessive epidermolysis bullosa simplex254183000
- Epidermolysis bullosa simplex of Ogna398071000
- Epidermolysis bullosa simplex, Ogna type398071000
- Autosomal dominant epidermolysis bullosa simplex398170002
- EBS 1398170002
- Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex403792007
- Ectodermal dysplasia skin fragility syndrome716699004
- Epidermolysis bullosa simplex due to plakophilin deficiency716699004
- McGrath syndrome716699004
- Epidermolysis bullosa simplex with circinate migratory erythema716700003
- Epidermolysis bullosa simplex co-occurrent with pyloric atresia716701004
- Epidermolysis bullosa simplex with pyloric atresia716701004
- Basal epidermolysis bullosa simplex723163000
- Epidermolysis bullosa simplex with muscular dystrophy723308003
- Limb girdle muscular dystrophy with epidermolysis bullosa simplex723308003
- EBS-AR KRT14 - epidermolysis bullosa simplex autosomal recessive keratin 14724206005
- KRT14 related epidermolysis bullosa simplex724206005
- Keratin 14 related epidermolysis bullosa simplex724206005
- Suprabasal epidermolysis bullosa simplex724840004
- DST (dystonin) related epidermolysis bullosa simplex773501006
- Epidermolysis bullosa simplex due to BP230 deficiency773501006
- Epidermolysis bullosa simplex due to exophilin 5 deficiency773503009
- Autosomal recessive epidermolysis bullosa simplex1156849001
- Intermediate epidermolysis bullosa simplex with cardiomyopathy1177176009
- Lethal acantholytic epidermolysis bullosa1230026002
- Lethal acantholytic erosive disorder1230026002
Frequently Asked Questions
What is the ICD-10 code for epidermolysis bullosa simplex?
The ICD-10-CM code for epidermolysis bullosa simplex is Q81.0. The full clinical description is "Epidermolysis bullosa simplex". Q81.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q81.0 mean?
ICD-10-CM code Q81.0 represents "Epidermolysis bullosa simplex". 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 Q81.0 a billable code?
Yes, Q81.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q81.0 in?
Q81.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q81.0?
Q81.0 has Excludes1 notes indicating codes that cannot be used together with it, including: Cockayne's syndrome (Q87.19).
What SNOMED CT codes does Q81.0 map to?
Q81.0 maps to 24 SNOMED CT concepts: 28828001, 398170002, 1156849001, 723163000, 773501006, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q81.0?
Q81.0 is linked to 1 UMLS Concept Unique Identifier: C0079298. 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.