Q82.1
BillableXeroderma pigmentosum
Xeroderma pigmentosum
Coding 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
Related Codes(8)
Q82.0Hereditary lymphedema
Q82.2Congenital cutaneous mastocytosis
Q82.3Incontinentia pigmenti
Q82.4Ectodermal dysplasia (anhidrotic)
Q82.5Congenital non-neoplastic nevus
Q82.6Congenital sacral dimple
Q82.8Other specified congenital malformations of skin
Q82.9Congenital malformation of skin, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(85)
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
Clinical Terms
- Kaposi dermatosis
- Xeroderma pigmentosum, group E
- Xeroderma pigmentosum, group B
- KAPOSIS DIS
- Pigmented xerodermoid
- Neurologic xeroderma pigmentosum
- Xeroderma pigmentosum, group G
- Angioma pigmentosum atrophicum
- Xeroderma pigmentosum and Cockayne syndrome complex
- pigmentosum xeroderma
- Pigmented epitheliomatosis
- Xeroderma pigmentosum, variant form
- KAPOSI DIS
- Xeroderma pigmentosum, group A
- Non-neurologic xeroderma pigmentosum
- Multiple malformation syndrome with senile-like appearance
- Xeroderma pigmentosum group E
- Kaposi's Disease
- Atrophoderma pigmentosum
- Xeroderma pigmentosum, group C
- Xeroderma pigmentosum group F
- Xeroderma pigmentosum, group D
- Xeroderma pigmentosum (disorder)
- Kaposis Disease
- Xeroderma pigmentosum group C
- Disorder of central nervous system due to xeroderma pigmentosum
- Xeroderma pigmentosum, group F
- Xeroderma of Kaposi
- Melanosis lenticularis progressiva
- Cockayne syndrome
- Xeroderma pigmentosum group D
- Xeroderma pigmentosum group A
- Xeroderma pigmentosum group G
- XP - Xeroderma pigmentosum
- Xeroderma pigmentosum XP variant
- Xeroderma pigmentosum group B
- Kaposi Disease
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.
How does Q82.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like xeroderma pigmentosum affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q82.1?
Q82.1 maps to the ICD-11 code: LD27.1 (Xeroderma pigmentosum).
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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.