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ICD-10-CM Codes
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L85-
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2023 ICD-10-CM Diagnosis Code L85.2
2023 ICD-10-CM Diagnosis Code L85.2
Keratosis punctata (palmaris et plantaris)
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- L85.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM L85.2 became effective on October 1, 2022.
- This is the American ICD-10-CM version of L85.2 - other international versions of ICD-10 L85.2 may differ.
The following code(s) above
L85.2 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
L85.2:
Approximate Synonyms
- Keratoderma punctata
- Keratosis punctata
Clinical Information
- A group of autosomal dominant, autosomal recessive, x-linked inherited or acquired disorders characterized by the thickening of the palms and soles due to hyperkeratosis.
- Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to hypertrophy of the stratum corneum (hyperkeratosis).
ICD-10-CM L85.2 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 606 Minor skin disorders with mcc
- 607 Minor skin disorders without mcc
Convert L85.2 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
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- Keratoderma, keratodermia (congenital) (palmaris et plantaris) (symmetrical) Q82.8
ICD-10-CM Diagnosis Code Q82.8
Other specified congenital malformations of skin
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
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- Ehlers-Danlos syndromes (Q79.6-)
- Keratosis L57.0
ICD-10-CM Diagnosis Code L57.0
Actinic keratosis
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Keratosis NOS
- Senile keratosis
- Solar keratosis
- punctata L85.2 (palmaris et plantaris)
ICD-10-CM Codes Adjacent To L85.2
L81.8 Other specified disorders of pigmentation
L81.9 Disorder of pigmentation, unspecified
L82.0 Inflamed seborrheic keratosis
L82.1 Other seborrheic keratosis
L84 Corns and callosities
L85 Other epidermal thickening
L85.0 Acquired ichthyosis
L85.1 Acquired keratosis [keratoderma] palmaris et plantaris
L85.2
Keratosis punctata (palmaris et plantaris)
L85.8 Other specified epidermal thickening
L85.9 Epidermal thickening, unspecified
L86 Keratoderma in diseases classified elsewhere
L87 Transepidermal elimination disorders
L87.0 Keratosis follicularis et parafollicularis in cutem penetrans
L87.1 Reactive perforating collagenosis
L87.2 Elastosis perforans serpiginosa
L87.8 Other transepidermal elimination disorders
L87.9 Transepidermal elimination disorder, unspecified
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.