2020 ICD-10-CM Diagnosis Code Q82.1

Xeroderma pigmentosum

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
  • Q82.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2020 edition of ICD-10-CM Q82.1 became effective on October 1, 2019.
  • This is the American ICD-10-CM version of Q82.1 - other international versions of ICD-10 Q82.1 may differ.
The following code(s) above Q82.1 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 Q82.1:
  • Q00-Q99
    2020 ICD-10-CM Range Q00-Q99

    Congenital malformations, deformations and chromosomal abnormalities

    Note
    • Codes from this chapter are not for use on maternal records
    Type 2 Excludes
    • inborn errors of metabolism (E70-E88)
    Congenital malformations, deformations and chromosomal abnormalities
  • Q82
    ICD-10-CM Diagnosis Code Q82

    Other congenital malformations of skin

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • acrodermatitis enteropathica (E83.2)
    • congenital erythropoietic porphyria (E80.0)
    • pilonidal cyst or sinus (L05.-)
    • Sturge-Weber (-Dimitri) syndrome (Q85.8)
    Other congenital malformations of skin
Clinical Information
  • A genetic condition characterized by a sensitivity to all sources of ultraviolet radiation.
  • A genetic condition marked by an extreme sensitivity to ultraviolet radiation, including sunlight. People with xeroderma pigmentosum are not able to repair skin damage from the sun and other sources of ultraviolet radiation, and have a very high risk of skin cancer.
  • A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ultraviolet rays as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged dna.
  • An inherited skin disorder characterized by photosensitivity with severe sunburn in infancy, the development of numerous pigmented spots resembling freckles, larger atrophic lesions associated with telangiectasis, and multiple solar keratoses. Transmitted in an autosomal recessive manner, xeroderma pigmentosa involves a defect in nucleotide excision repair (ner), leading to deficient repair of dna damaged by uv radiation and chromosome breakage. Individuals with this disease develop multiple malignant cutaneous neoplasms at an early age and may suffer from severe ophthalmic and neurologic abnormalities.
  • Rare pigmentary atrophic autosomal recessive disease manifested as an extreme photosensitivity to ultraviolet light as the result of a deficiency in the enzyme that permits excisional repair of utraviolet damaged dna.
Present On Admission
POA 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.
  • Q82.1 is considered exempt from POA reporting.
ICD-10-CM Q82.1 is grouped within Diagnostic Related Group(s) (MS-DRG v37.0):
  • 606 Minor skin disorders with mcc
  • 607 Minor skin disorders without mcc
  • 795 Normal newborn

Convert Q82.1 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
Code annotations containing back-references to Q82.1:
  • Type 1 Excludes: E79
    ICD-10-CM Diagnosis Code E79

    Disorders of purine and pyrimidine metabolism

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
  • Type 2 Excludes: G11.3
    ICD-10-CM Diagnosis Code G11.3

    Cerebellar ataxia with defective DNA repair

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Ataxia telangiectasia [Louis-Bar]
    Type 2 Excludes
    • Cockayne's syndrome (Q87.19)
    • other disorders of purine and pyrimidine metabolism (E79.-)
    • xeroderma pigmentosum (Q82.1)

Diagnosis Index entries containing back-references to Q82.1:
  • Atrophoderma, atrophodermia (of) L90.9
    ICD-10-CM Diagnosis Code L90.9

    Atrophic disorder of skin, unspecified

      2016 2017 2018 2019 2020 Billable/Specific Code
    • pigmentosum Q82.1
  • Epitheliomatosis pigmented Q82.1
  • Kaposi's
    • dermatosis Q82.1 (xeroderma pigmentosum)
  • Melanosis L81.4
    ICD-10-CM Diagnosis Code L81.4

    Other melanin hyperpigmentation

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Lentigo
    • lenticularis progressiva Q82.1
  • Xeroderma - see also Ichthyosis
    • pigmentosum Q82.1

ICD-10-CM Codes Adjacent To Q82.1
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
Q82.0 Hereditary lymphedema
Q82.1 Xeroderma pigmentosum
Q82.2 Congenital cutaneous mastocytosis
Q82.3 Incontinentia pigmenti
Q82.4 Ectodermal dysplasia (anhidrotic)
Q82.5 Congenital non-neoplastic nevus
Q82.6 Congenital sacral dimple
Q82.8 Other specified congenital malformations of skin
Q82.9 Congenital malformation of skin, unspecified
Q83 Congenital malformations of breast
Q83.0 Congenital absence of breast with absent nipple
Q83.1 Accessory breast

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.