Q61Cystic kidney disease
Code usage status
Primary diagnosis
Select a more specific code
Apply only when it matches the confirmed diagnosis and the documented clinical record.
Specificity
Do not use Q61 directly
Use the most specific code supported by the record.
- Group Q60-Q64
- Congenital malformations of the urinary system
- Official Vietnamese name
- Bệnh nang thận
- Additional WHO coding guidance
- Excl.: cyst of kidney (acquired) (N28.1) Potter syndrome (Q60.6)
Related Q61 codes
Q61.0
Primary diagnosis candidate
Congenital single renal cyst
Q61.1
Primary diagnosis candidate
Polycystic kidney, autosomal recessive
Q61.2
Primary diagnosis candidate
Polycystic kidney, autosomal dominant
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.
