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ICD-10-CM Codes
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Q00-Q99
Congenital malformations, deformations and chromosomal abnormalities
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Q80-Q89
Other congenital malformations
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Q82-
Other congenital malformations of skin
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2021 ICD-10-CM Diagnosis Code Q82
2021 ICD-10-CM Diagnosis Code Q82
Other congenital malformations of skin
2016 2017 2018 2019 2020 2021 Non-Billable/Non-Specific Code
- Q82 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
- The 2021 edition of ICD-10-CM Q82 became effective on October 1, 2020.
- This is the American ICD-10-CM version of Q82 - other international versions of ICD-10 Q82 may differ.
Type 1 ExcludesType 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 2019 2020 2021 Billable/Specific Code
Applicable To- Acrodermatitis enteropathica
- congenital erythropoietic porphyria (
ICD-10-CM Diagnosis Code E80.0
Hereditary erythropoietic porphyria
2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To- Congenital erythropoietic porphyria
- Erythropoietic protoporphyria
- 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
- Sturge-Weber (-Dimitri) syndrome (
ICD-10-CM Diagnosis Code Q85.8
Other phakomatoses, not elsewhere classified
2016 2017 2018 2019 2020 2021 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)
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:
- 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
ICD-10-CM Codes Adjacent To Q82
Q80.3 Congenital bullous ichthyosiform erythroderma
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.
