Q82.1
BillableXeroderma pigmentosum
Xeroderma pigmentosum
Status
Billable / Specific
Parent Code
Q82Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
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
- Xeroderma pigmentosum group B1073003
- Xeroderma pigmentosum, group B1073003
- Non-neurologic xeroderma pigmentosum7806002
- Multiple malformation syndrome with senile-like appearance12674005
- Cockayne syndrome21086008
- Xeroderma pigmentosum group C25784009
- Xeroderma pigmentosum, group C25784009
- Xeroderma pigmentosum group G36454001
- Xeroderma pigmentosum, group G36454001
- Xeroderma pigmentosum group F42530008
- Xeroderma pigmentosum, group F42530008
- Xeroderma pigmentosum group A43477006
- Xeroderma pigmentosum, group A43477006
- Angioma pigmentosum atrophicum44600005
- Atrophoderma pigmentosum44600005
- Kaposi dermatosis44600005
- Melanosis lenticularis progressiva44600005
- Pigmented epitheliomatosis44600005
- XP - Xeroderma pigmentosum44600005
- Xeroderma of Kaposi44600005
- Xeroderma pigmentosum44600005
- Xeroderma pigmentosum group E56048001
- Xeroderma pigmentosum, group E56048001
- Xeroderma pigmentosum group D68637004
- Xeroderma pigmentosum, group D68637004
- Disorder of central nervous system due to xeroderma pigmentosum73663008
- Neurologic xeroderma pigmentosum73663008
- Pigmented xerodermoid88877002
- Xeroderma pigmentosum XP variant88877002
- Xeroderma pigmentosum, variant form88877002
- Xeroderma pigmentosum and Cockayne syndrome complex719819004
UMLS
- Angioma pigmentosum atrophicumC0043346
- Atrophoderma pigmentosumC0043346
- KAPOSI DISC0043346
- KAPOSIS DISC0043346
- Kaposi DiseaseC0043346
- Kaposi dermatosisC0043346
- Kaposi's DiseaseC0043346
- Kaposis DiseaseC0043346
- Melanosis lenticularis progressivaC0043346
- Pigmented epitheliomatosisC0043346
- XP - Xeroderma pigmentosumC0043346
- Xeroderma PigmentosumC0043346
- Xeroderma of KaposiC0043346
- Xeroderma pigmentosumC0043346
- Xeroderma pigmentosum (disorder)C0043346
- pigmentosum xerodermaC0043346
- xeroderma pigmentosumC0043346
Frequently Asked Questions
What is the ICD-10 code for xeroderma pigmentosum?
The ICD-10-CM code for xeroderma pigmentosum is Q82.1. The full clinical description is "Xeroderma pigmentosum". Q82.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q82.1 mean?
ICD-10-CM code Q82.1 represents "Xeroderma pigmentosum". 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 Q82.1 a billable code?
Yes, Q82.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q82.1 in?
Q82.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q82.1?
Q82.1 has Excludes1 notes indicating codes that cannot be used together with it, including: acrodermatitis enteropathica (E83.2); congenital erythropoietic porphyria (E80.0); pilonidal cyst or sinus (L05.-); and 1 more.
What SNOMED CT codes does Q82.1 map to?
Q82.1 maps to 14 SNOMED CT concepts: 44600005, 21086008, 73663008, 12674005, 7806002, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q82.1?
Q82.1 is linked to 1 UMLS Concept Unique Identifier: C0043346. 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.