ICD-10-CM Codes
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities
Q80-Q89 Other congenital malformations
Q82- Other congenital malformations of skin

2019 ICD-10-CM Diagnosis Code Q82

Other congenital malformations of skin

2016

2017

2018

2019

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 2019 edition of ICD-10-CM Q82 became effective on October 1, 2018.
This is the American ICD-10-CM version of Q82 - other international versions of ICD-10 Q82 may differ.

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. 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
Applicable To
- Acrodermatitis enteropathica
E83.2
)
congenital erythropoietic porphyria (
ICD-10-CM Diagnosis Code E80.0
Hereditary erythropoietic porphyria
Applicable To
- Congenital erythropoietic porphyria
- Erythropoietic protoporphyria
E80.0
)
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
L05.-
)
Sturge-Weber (-Dimitri) syndrome (
ICD-10-CM Diagnosis Code Q85.8
Other phakomatoses, not elsewhere classified
Applicable To
- Peutz-Jeghers Syndrome
- Sturge-Weber(-Dimitri) syndrome
- von Hippel-Lindau syndrome
Type 1 Excludes
- Meckel-Gruber syndrome (Q61.9)
Q85.8
)

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:

Q00-Q99
2019 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

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

ICD-10-CM Codes Adjacent To Q82

Q80.3 Congenital bullous ichthyosiform erythroderma

Q80.4 Harlequin fetus

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.

2019 ICD-10-CM Diagnosis Code Q82

Other congenital malformations of skin

Disorders of zinc metabolism

Hereditary erythropoietic porphyria

Other phakomatoses, not elsewhere classified

Congenital malformations, deformations and chromosomal abnormalities