Q82Other congenital malformations of skin
Code usage status
Primary diagnosis
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Apply only when it matches the confirmed diagnosis and the documented clinical record.
Specificity
Do not use Q82 directly
Use the most specific code supported by the record.
- Group Q80-Q89
- Other congenital malformations
- Official Vietnamese name
- Dị tật bẩm sinh khác của da
- Additional WHO coding guidance
- Excl.: acrodermatitis enteropathica (E83.2) congenital erythropoietic porphyria (E80.0) pilonidal cyst or sinus (L05.-) Sturge-Weber(- Dimitri) syndrome (Q85.8)
Related Q82 codes
Q82.0
Primary diagnosis candidate
Hereditary lymphoedema
Q82.1
Primary diagnosis candidate
Xeroderma pigmentosum
Q82.2
Primary diagnosis candidate
Mastocytosis
Q82.3
Primary diagnosis candidate
Incontinentia pigmenti
Q82.4
Primary diagnosis candidate
Ectodermal dysplasia (anhidrotic)
Q82.5
Primary diagnosis candidate
Congenital non- neoplastic naevus
Q82.8
Primary diagnosis candidate
Other specified congenital malformations of skin
Q82.9
Primary diagnosis candidate
Congenital malformation of skin, unspecified
Clinical record checklist
View coding guide →- Confirm that the code matches the final documented diagnosis.
- Use one primary-diagnosis code and record only relevant additional conditions.
- Review Ministry indicators, inclusions, exclusions and notes.
- Do not infer a diagnosis beyond the clinical record.
2026 regulatory basis
Indicators are taken from columns 24–29 of the classification accompanying Circular 06/2026/TT-BYT, cross-referenced with Decision 1849/QĐ-BYT and Official Dispatch 4059/BYT-BH.
