VITiếng Việt
ICD-10 Vietnam

Q61.2Polycystic kidney, autosomal dominant

Code usage status

Primary diagnosis

May be used as the primary diagnosis

Apply only when it matches the confirmed diagnosis and the documented clinical record.

Specificity

Complete code in the classification

Use when the diagnosis matches and no exclusion applies.

Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
Group Q60-Q64
Congenital malformations of the urinary system
Official Vietnamese name
Bệnh thận đa nang, di truyền trội trên nhiễm sắc thể thường
Additional WHO coding guidance
Polycystic kidney, adult type

Related Q61 codes

Q61 Cystic kidney disease Q61.0 Primary diagnosis candidate Congenital single renal cyst Q61.1 Primary diagnosis candidate Polycystic kidney, autosomal recessive Q61.3 Primary diagnosis candidate Polycystic kidney, unspecified Q61.4 Primary diagnosis candidate Renal dysplasia Q61.5 Primary diagnosis candidate Medullary cystic kidney Q61.8 Primary diagnosis candidate Other cystic kidney diseases Q61.9 Primary diagnosis candidate Cystic kidney disease, 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.