2020 ICD-10-CM Diagnosis Code Q82.8

Other specified congenital malformations of skin

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
  • Q82.8 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 Q82.8 became effective on October 1, 2019.
  • This is the American ICD-10-CM version of Q82.8 - other international versions of ICD-10 Q82.8 may differ.
Applicable To
  • Abnormal palmar creases
  • Accessory skin tags
  • Benign familial pemphigus [Hailey-Hailey]
  • Congenital poikiloderma
  • Cutis laxa (hyperelastica)
  • Dermatoglyphic anomalies
  • Inherited keratosis palmaris et plantaris
  • Keratosis follicularis [Darier-White]
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 Q82.8. 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.
  • Ehlers-Danlos syndrome (
    ICD-10-CM Diagnosis Code Q79.6

    Ehlers-Danlos syndromes

      2016 2017 2018 2019 2020 - Converted to Parent Code Non-Billable/Non-Specific Code
    Q79.6-
    )
The following code(s) above Q82.8 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 Q82.8:
  • 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
Approximate Synonyms
  • Abnormal dermatoglyphic pattern
  • Abnormal gluteal crease
  • Abnormal palmar creases
  • Accessory skin tag, congenital
  • Acrokeratosis verruciformis of hopf
  • Acrokeratosis verruciforms
  • Anomaly of skin pigment, congenital
  • Aplasia cutis
  • Aplasia cutis congenita
  • Bloom syndrome
  • Congenital accessory skin tag
  • Congenital keratoderma
  • Congenital keratosis follicularis
  • Congenital keratosis pilaris
  • Congenital pigmentary skin anomalies
  • Congenital scar
  • Congenital skin contracture
  • Dariers disease
  • Dermatoglyphic anomalies
  • Dyskeratosis congenita
  • Familial benign pemphigus
  • Goltz syndrome
  • Goltz-gorlin (dermal hypoplasia) syndrome
  • Hailey disease
  • Hereditary benign acanthosis nigricans
  • Howel evans syndrome
  • Howel-evans' syndrome
  • Keratoderma, congenital
  • Keratosis follicularis
  • Keratosis pilaris, congenital
  • Mongolian spot
  • Mongolian spot (blue/gray skin discoloration)
  • Pachydermoperiostosis syndrome
  • Porokeratosis
  • Porokeratosis (skin condition)
  • Porokeratosis of mibelli
  • Pseudoxanthoma elasticum
  • Sacral dimple
  • Scar, congenital
  • Touraine-solente-gole syndrome
Clinical Information
  • A congenital or acquired disorder affecting the elastic fibers of the skin. It is characterized by loss of elasticity resulting in loosening and folding of the skin.
  • A group of connective tissue diseases in which skin hangs in loose pendulous folds. It is believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation. Cutis laxa is usually a genetic disease, but acquired cases have been reported. (from Dorland, 27th ed)
  • A rare inherited disorder that affects the skin and many other parts of the body, including the bones, eyes, nose, hair, nails, teeth, testes, and ovaries. People with rothmund-thomson syndrome have an increased risk of osteosarcoma (bone cancer).
  • An autosomal dominant disorder characterized by a history of multiple relapses and remissions of pemphigus lesions.
  • An autosomal dominantly inherited skin disorder characterized by recurrent eruptions of vesicles and bullae mainly on the neck, axillae, and groin. Mutations in the atp2c1 gene (encoding the secretory pathway ca2++/mn2++ atpase 1 (spca1)) cause this disease. It is clinically and histologically similar to darier disease - both have abnormal, unstable desmosomes between keratinocytes and defective calcium-transporting atpases. It is unrelated to pemphigus vulgaris though it closely resembles that disease.
  • An autosomal recessive inherited syndrome usually caused by mutations in the recql4 gene. It is characterized by poikilodermatous skin changes, sparse hair, cataracts, small stature, skeletal abnormalities, and an increased predisposition to cancer, particularly osteosarcoma.
  • An autosomal recessive syndrome occurring principally in females, characterized by the presence of reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often accompanied by juvenile cataracts, saddle nose, congenital bone defects, disturbances in the growth of hair; nails; and teeth; and hypogonadism.
  • Group of connective tissue diseases in which skin hangs in loose pendulous folds; believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation; usually a genetic disease, but acquired cases have been reported.
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.
  • Q82.8 is considered exempt from POA reporting.
ICD-10-CM Q82.8 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 Q82.8 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 Q82.8:
  • Type 1 Excludes: E79
    , L11.0
    , L85.1
    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
    ICD-10-CM Diagnosis Code L11.0

    Acquired keratosis follicularis

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • keratosis follicularis (congenital) [Darier-White] (Q82.8)
    ICD-10-CM Diagnosis Code L85.1

    Acquired keratosis [keratoderma] palmaris et plantaris

      2016 2017 2018 2019 2020 Billable/Specific Code
    Type 1 Excludes
    • inherited keratosis palmaris et plantaris (Q82.8)

Diagnosis Index entries containing back-references to Q82.8:
  • Abnormal, abnormality, abnormalities - see also Anomaly
    • palmar creases Q82.8
  • Acanthosis (acquired) (nigricans) L83
    ICD-10-CM Diagnosis Code L83

    Acanthosis nigricans

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Confluent and reticulated papillomatosis
    • benign Q82.8
    • congenital Q82.8
  • Accessory (congenital)
    • skin tags Q82.8
  • Angiomatosis Q82.8
  • Anomaly, anomalous (congenital) (unspecified type) Q89.9
    ICD-10-CM Diagnosis Code Q89.9

    Congenital malformation, unspecified

      2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    Applicable To
    • Congenital anomaly NOS
    • Congenital deformity NOS
    • pigmentation L81.9
      ICD-10-CM Diagnosis Code L81.9

      Disorder of pigmentation, unspecified

        2016 2017 2018 2019 2020 Billable/Specific Code
      • congenital Q82.8
    • dermatoglyphic Q82.8
    • simian crease Q82.8
  • Bloom Q82.8 (-Machacek)(-Torre)
  • Brugsch's syndrome Q82.8
  • Cutis - see also condition
  • Darier (-White) disease (congenital) Q82.8
  • Dermatolysis (exfoliativa) (congenital) Q82.8
  • Dermatomegaly NEC Q82.8
  • Dyskeratosis L85.8
    ICD-10-CM Diagnosis Code L85.8

    Other specified epidermal thickening

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Cutaneous horn
    • congenital Q82.8
  • Dysplasia - see also Anomaly
    • ectodermal (anhidrotic) (congenital) (hereditary) Q82.4
      ICD-10-CM Diagnosis Code Q82.4

      Ectodermal dysplasia (anhidrotic)

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Type 1 Excludes
      • Ellis-van Creveld syndrome (Q77.6)
      • hydrotic Q82.8
  • Elastic skin Q82.8
  • Elastoma (juvenile) Q82.8
  • Gyrate scalp Q82.8
  • Hailey-Hailey disease Q82.8
  • Hyperkeratosis L85.9
    - see also Keratosis
    ICD-10-CM Diagnosis Code L85.9

    Epidermal thickening, unspecified

      2016 2017 2018 2019 2020 Billable/Specific Code
  • Hypoplasia, hypoplastic
    • focal dermal Q82.8
    • skin Q82.8
  • Ichthyosis (congenital) Q80.9
    ICD-10-CM Diagnosis Code Q80.9

    Congenital ichthyosis, unspecified

      2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    • palmaris and plantaris Q82.8
  • India rubber skin Q82.8
  • Keratoderma, keratodermia (congenital) (palmaris et plantaris) (symmetrical) Q82.8
  • Keratoma L57.0
    ICD-10-CM Diagnosis Code L57.0

    Actinic keratosis

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Keratosis NOS
    • Senile keratosis
    • Solar keratosis
    • palmaris and plantaris hereditarium Q82.8
  • Keratosis L57.0
    ICD-10-CM Diagnosis Code L57.0

    Actinic keratosis

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Keratosis NOS
    • Senile keratosis
    • Solar keratosis
  • Lax, laxity - see also Relaxation
    • skin (acquired) L57.4
      ICD-10-CM Diagnosis Code L57.4

      Cutis laxa senilis

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Elastosis senilis
      • congenital Q82.8
  • Lichen L28.0
    ICD-10-CM Diagnosis Code L28.0

    Lichen simplex chronicus

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Circumscribed neurodermatitis
    • Lichen NOS
  • Melanocytosis, neurocutaneous Q82.8
  • Mibelli's disease Q82.8 (porokeratosis)
  • Naegeli's
    • disease Q82.8
  • Pachydermatocele Q82.8 (congenital)
  • Particolored infant Q82.8
  • Pemphigus L10.9
    ICD-10-CM Diagnosis Code L10.9

    Pemphigus, unspecified

      2016 2017 2018 2019 2020 Billable/Specific Code
    • benign familial Q82.8 (chronic)
  • Pigmentation (abnormal) (anomaly) L81.9
    ICD-10-CM Diagnosis Code L81.9

    Disorder of pigmentation, unspecified

      2016 2017 2018 2019 2020 Billable/Specific Code
    • lids, congenital Q82.8
    • scrotum, congenital Q82.8
  • Poikiloderma L81.6
    ICD-10-CM Diagnosis Code L81.6

    Other disorders of diminished melanin formation

      2016 2017 2018 2019 2020 Billable/Specific Code
    • congenital Q82.8
  • Porokeratosis Q82.8
  • Pseudoxanthoma elasticum Q82.8
  • Rothmund Q82.8 (-Thomson)
  • Siemens' syndrome Q82.8 (ectodermal dysplasia)
  • Syndrome - see also Disease
    • telangiectasic-pigmentation-cataract Q82.8
  • Tag (hypertrophied skin) (infected) L91.8
    ICD-10-CM Diagnosis Code L91.8

    Other hypertrophic disorders of the skin

      2016 2017 2018 2019 2020 Billable/Specific Code
    • skin L91.8
      ICD-10-CM Diagnosis Code L91.8

      Other hypertrophic disorders of the skin

        2016 2017 2018 2019 2020 Billable/Specific Code
      • accessory Q82.8 (congenital)
      • congenital Q82.8
  • Tylosis (acquired) L84
    ICD-10-CM Diagnosis Code L84

    Corns and callosities

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Callus
    • Clavus

ICD-10-CM Codes Adjacent To Q82.8
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
Q83.2 Absent nipple
Q83.3 Accessory nipple
Q83.8 Other congenital malformations of breast
Q83.9 Congenital malformation of breast, unspecified
Q84 Other congenital malformations of integument
Q84.0 Congenital alopecia

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