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ICD-10-CM Codes
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Q00-Q99
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Q80-Q89
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Q80-
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2023 ICD-10-CM Diagnosis Code Q80.3
2023 ICD-10-CM Diagnosis Code Q80.3
Congenital bullous ichthyosiform erythroderma
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
- Q80.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM Q80.3 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q80.3 - other international versions of ICD-10 Q80.3 may differ.
The following code(s) above
Q80.3 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
Q80.3:
- Congenital ichthyosiform erythroderma
- Dominant congenital ichthyosiform erythroderma
- Ichthyosiform erythroderma
Clinical Information
- A form of congenital ichthyosis inherited as an autosomal dominant trait and characterized by erythroderma and severe hyperkeratosis. It is manifested at birth by blisters followed by the appearance of thickened, horny, verruciform scales over the entire body, but accentuated in flexural areas. Mutations in the genes that encode keratin-1 and keratin-10 have been associated with this disorder.
- An autosomal dominant inherited skin disorder caused by mutations in the krt1 and krt10 genes. It is manifested at birth and is characterized by generalized erythema, skin blisters and skin fragility.
Present On AdmissionPOA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
- Q80.3 is considered exempt from POA reporting.
ICD-10-CM Q80.3 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 606 Minor skin disorders with mcc
- 607 Minor skin disorders without mcc
Convert Q80.3 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- Erythema, erythematous (infectional) (inflammation) L53.9
ICD-10-CM Diagnosis Code L53.9
Erythematous condition, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Erythema NOS
- Erythroderma NOS
- ichthyosiforme congenitum bullous Q80.3
- Erythroderma (secondary) L53.9 - see also Erythema
ICD-10-CM Diagnosis Code L53.9
Erythematous condition, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Erythema NOS
- Erythroderma NOS
- bullous ichthyosiform, congenital Q80.3
- ichthyosiform, congenital Q80.3 (bullous)
ICD-10-CM Codes Adjacent To Q80.3
Q79.61 Classical Ehlers-Danlos syndrome
Q79.62 Hypermobile Ehlers-Danlos syndrome
Q79.63 Vascular Ehlers-Danlos syndrome
Q79.69 Other Ehlers-Danlos syndromes
Q79.8 Other congenital malformations of musculoskeletal system
Q79.9 Congenital malformation of musculoskeletal system, unspecified
Q80 Congenital ichthyosis
Q80.0 Ichthyosis vulgaris
Q80.1 X-linked ichthyosis
Q80.2 Lamellar ichthyosis
Q80.3
Congenital bullous ichthyosiform erythroderma
Q80.8 Other congenital ichthyosis
Q80.9 Congenital ichthyosis, unspecified
Q81 Epidermolysis bullosa
Q81.0 Epidermolysis bullosa simplex
Q81.1 Epidermolysis bullosa letalis
Q81.2 Epidermolysis bullosa dystrophica
Q81.8 Other epidermolysis bullosa
Q81.9 Epidermolysis bullosa, unspecified
Q82 Other congenital malformations of skin
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
