4 result found:

Other specified congenital malformations of skin
ICD-10-CM Diagnosis Code Q82.8

Other specified congenital malformations of skin

    2016 2017 2018 2019 2020 2021 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-)
Acquired keratosis follicularis
keratosis follicularis (congenital) [Darier-White] (Q82.8)
ICD-10-CM Diagnosis Code L11.0

Acquired keratosis follicularis

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Type 1 Excludes
  • keratosis follicularis (congenital) [Darier-White] (Q82.8)
Acquired keratosis [keratoderma] palmaris et plantaris
Acquired keratoderma; Acquired plantar keratoderma; Keratoderma blennorrhagicum; Keratoderma foot, acquired; Keratoderma, acquired; inherited keratosis palmaris et plantaris (Q82.8)
ICD-10-CM Diagnosis Code L85.1

Acquired keratosis [keratoderma] palmaris et plantaris

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Type 1 Excludes
  • inherited keratosis palmaris et plantaris (Q82.8)
Disorders of purine and pyrimidine metabolism
Ataxia-telangiectasia (Q87.19); Bloom's syndrome (Q82.8); Cockayne's syndrome (Q87.19); calculus of kidney (N20.0); combined immunodeficiency disorders (D81.-); Fanconi's anemia (D61.09); gout (M1A.-, M10.-); orotaciduric anemia (D53.0); progeria (E34.8); Werner's syndrome (E34.8); xeroderma pigmentosum (Q82.1)
ICD-10-CM Diagnosis Code E79
  • E79 Disorders of purine and pyrimidine metabolism...
    • E79.0 Hyperuricemia without signs of inflammatory a...
    • E79.1 Lesch-Nyhan syndrome
    • E79.2 Myoadenylate deaminase deficiency
    • E79.8 Other disorders of purine and pyrimidine meta...
    • E79.9 Disorder of purine and pyrimidine metabolism,...