Other congenital malformations of skin Q82-

Type 1 Excludes
Type 1 Excludes Help
A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as Q82. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
  • acrodermatitis enteropathica (
    ICD-10-CM Diagnosis Code E83.2

    Disorders of zinc metabolism

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    Applicable To
    • Acrodermatitis enteropathica
    E83.2
    )
  • congenital erythropoietic porphyria (
    ICD-10-CM Diagnosis Code E80.0

    Hereditary erythropoietic porphyria

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    Applicable To
    • Congenital erythropoietic porphyria
    • Erythropoietic protoporphyria
    E80.0
    )
  • pilonidal cyst or sinus (
    ICD-10-CM Diagnosis Code L05
    • L05 Pilonidal cyst and sinus
      • L05.0 Pilonidal cyst and sinus with abscess
        • L05.01 Pilonidal cyst with abscess
        • L05.02 Pilonidal sinus with abscess
      • L05.9 Pilonidal cyst and sinus without abscess
        • L05.91 Pilonidal cyst without abscess
        • L05.92 Pilonidal sinus without abscess
    L05.-
    )
  • Sturge-Weber (-Dimitri) syndrome (
    ICD-10-CM Diagnosis Code Q85.89

    Other phakomatoses, not elsewhere classified

      2023 - New Code Billable/Specific Code POA Exempt
    Applicable To
    • Peutz-Jeghers syndrome
    • Sturge-Weber(-Dimitri) syndrome
    Q85.89
    )
Codes
  • 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