Q80.3
BillableCongenital bullous ichthyosiform erythroderma
Congenital bullous ichthyosiform erythroderma
Status
Billable / Specific
Parent Code
Q80Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Dwarfism-ichthyosiform erythroderma-mental deficiency syndrome2355008
- Rud syndrome2355008
- Rud's syndrome2355008
- Alligator skin254156001
- Congenital ichthyosiform erythroderma254156001
- BIE - Bullous ichthyosiform erythroderma254167000
- Bullous ichthyosiform erythroderma254167000
- Bullous ichthyosis254167000
- Congenital bullous ichthyosiform erythroderma254167000
- Dominant ichthyosis vulgaris254167000
- Epidermolytic hyperkeratosis254167000
- Localised bullous ichthyosiform erythroderma254168005
- Localized bullous ichthyosiform erythroderma254168005
- Ichthyosis bullosa of Siemens254169002
- Congenital non bullous ichthyosiform erythroderma267372009
- Ichthyosiform dermatosis268282005
- Ichthyosiform erythroderma268282005
- Autosomal dominant ichthyosis402770002
- CRIE - Congenital reticular ichthyosiform erythroderma703504006
- Congenital reticular ichthyosiform erythroderma703504006
- Ichthyosis variegata703504006
- Ichthyosis with confetti703504006
- Genetically determined skin fragility724851004
- Hereditary skin fragility724851004
UMLS
- BCIEC0079153
- BIEC0079153
- BIE - Bullous ichthyosiform erythrodermaC0079153
- BULLOUS CONGEN ICHTHYOSIFORM ERYTHRODERMAC0079153
- BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMAC0079153
- BULLOUS ERYTHRODERMA ICHTHYOSIFORMIS CONGENITA OF BROCQC0079153
- BULLOUS ICHTHYOSIFORM ERYTHRODERMAC0079153
- Bullous Congenital Ichthyosiform ErythrodermaC0079153
- Bullous Erythroderma IchthyosiformeC0079153
- Bullous Erythroderma IchthyosiformesC0079153
- Bullous Erythroderma Ichthyosiformis Congenita of BrocqC0079153
- Bullous Ichthyosiform ErythrodermaC0079153
- Bullous Ichthyosiform Erythroderma CongenitalC0079153
- Bullous Ichthyosiform ErythrodermasC0079153
- Bullous congenital ichthyosiform erythrodermaC0079153
- Bullous erythroderma ichthyosiformeC0079153
- Bullous erythroderma ichthyosiformis congenita of BrocqC0079153
- Bullous ichthyosiform erythrodermaC0079153
- Bullous ichthyosiform erythroderma (disorder)C0079153
- Bullous ichthyosisC0079153
- CONGEN BULLOUS ICHTHYOSIFORM ERYTHRODERMAC0079153
- Congenital Bullous Ichthyosiform ErythrodermaC0079153
- Congenital Ichthyosiform Erythroderma, BullousC0079153
- Congenital bullous ichthyosiform erythrodermaC0079153
- Dominant ichthyosis vulgarisC0079153
- EHKC0079153
- EPIDERMOLYTIC ICHTHYOSISC0079153
- Epidermolytic HyperkeratosesC0079153
- Epidermolytic HyperkeratosisC0079153
- Epidermolytic IchthyosisC0079153
- Epidermolytic hyperkeratosisC0079153
- Epidermolytic ichthyosisC0079153
- Epidermolytic palmoplantar hyperkeratosisC0079153
- Erythroderma Ichthyosiforme, BullousC0079153
- Erythroderma Ichthyosiformes, BullousC0079153
- Erythroderma, Bullous IchthyosiformC0079153
- Erythrodermas, Bullous IchthyosiformC0079153
- Hyperkeratoses, EpidermolyticC0079153
- Hyperkeratosis, EpidermolyticC0079153
- Hyperkeratosis, epidermolyticC0079153
- ICHTHYOSIFORM ERYTHRODERMA BULLOUS CONGENC0079153
- Ichthyosiform Erythroderma, BullousC0079153
- Ichthyosiform Erythroderma, Bullous CongenitalC0079153
- Ichthyosiform Erythrodermas, BullousC0079153
- Ichthyosiforme, Bullous ErythrodermaC0079153
- Ichthyosiformes, Bullous ErythrodermaC0079153
- epidermolytic hyperkeratosisC0079153
Frequently Asked Questions
What is the ICD-10 code for congenital bullous ichthyosiform erythroderma?
The ICD-10-CM code for congenital bullous ichthyosiform erythroderma is Q80.3. The full clinical description is "Congenital bullous ichthyosiform erythroderma". Q80.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q80.3 mean?
ICD-10-CM code Q80.3 represents "Congenital bullous ichthyosiform erythroderma". 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 Q80.3 a billable code?
Yes, Q80.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q80.3 in?
Q80.3 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q80.3?
Q80.3 has Excludes1 notes indicating codes that cannot be used together with it, including: Refsum's disease (G60.1).
What SNOMED CT codes does Q80.3 map to?
Q80.3 maps to 10 SNOMED CT concepts: 254156001, 402770002, 254167000, 703504006, 267372009, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q80.3?
Q80.3 is linked to 1 UMLS Concept Unique Identifier: C0079153. 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.