- Q82.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM Q82.8 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q82.8 – other international versions of ICD-10 Q82.8 may differ.
ICD-10-CM Q82.8 is grouped within Diagnostic Related Group(s):
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-)
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 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
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to Q82.8:
- palmar creases > Abnormal, abnormality, abnormalities
- benign > Acanthosis (acquired) (nigricans) L83
- congenital > Acanthosis (acquired) (nigricans) L83
- skin tags > Accessory (congenital)
- dermatoglyphic > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- congenital > pigmentation L81.9
- simian crease > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- hyperelastica > Cutis
- verticis gyrata > Cutis
- congenital > Dyskeratosis L85.8
- hydrotic > ectodermal (anhidrotic) (congenital) (hereditary) Q82.4
- follicularis > Hyperkeratosis L85.9
- focal dermal > Hypoplasia, hypoplastic
- skin > Hypoplasia, hypoplastic
- palmaris and plantaris > Ichthyosis (congenital) Q80.9
- palmaris and plantaris hereditarium > Keratoma L57.0
- follicularis > Keratosis L57.0
- congenita > follicularis Q82.8
- spinulosa (decalvans) > follicularis Q82.8
- palmaris et plantaris (inherited) (symmetrical) > Keratosis L57.0
- vegetans > Keratosis L57.0
- congenital > skin (acquired) L57.4
- congenital > Lichen L28.0
- pilaris > Lichen L28.0
- disease > Naegeli\’s
- benign familial (chronic) > Pemphigus L10.9
- lids, congenital > Pigmentation (abnormal) (anomaly) L81.9
- scrotum, congenital > Pigmentation (abnormal) (anomaly) L81.9
- congenital > Poikiloderma L81.6
- telangiectasic-pigmentation-cataract > Syndrome
- accessory (congenital) > skin L91.8
- congenital > skin L91.8
- palmaris et plantaris (congenital) (inherited) > Tylosis (acquired) L84