2017/18 ICD-10-CM Diagnosis Code Q82

Other congenital malformations of skin

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 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 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 Q85.8

    Other phakomatoses, not elsewhere classified

      2016 2017 2018 Billable/Specific Code POA Exempt
    Applicable To
    • Peutz-Jeghers Syndrome
    • Sturge-Weber(-Dimitri) syndrome
    • von Hippel-Lindau syndrome
    Type 1 Excludes
    • Meckel-Gruber syndrome (Q61.9)
    Q85.8
    )
The following code(s) above Q82 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:
  • Q00-Q99
    2018 ICD-10-CM Range Q00-Q99

    Congenital malformations, deformations and chromosomal abnormalities

    Note
    • Codes from this chapter are not for use on maternal or fetal records
    Type 2 Excludes
    • inborn errors of metabolism (E70-E88)
    Congenital malformations, deformations and chromosomal abnormalities
Code History
ICD-10-CM Codes Adjacent To Q82
Q80.3 Congenital bullous ichthyosiform erythroderma
Q80.4 Harlequin fetus
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

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