Q60Renal agenesis and other reduction defects of kidney
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 Q60 directly
Use the most specific code supported by the record.
- Group Q60-Q64
- Congenital malformations of the urinary system
- Official Vietnamese name
- Dị tật bất sản và/hoặc khuyết thiếu khác của thận
- Additional WHO coding guidance
- Incl.: atrophy of kidney: congenital infantile congenital absence of kidney
Related Q60 codes
Q60.0
Primary diagnosis candidate
Renal agenesis, unilateral
Q60.1
Primary diagnosis candidate
Renal agenesis, bilateral
Q60.2
Primary diagnosis candidate
Renal agenesis, unspecified
Q60.3
Primary diagnosis candidate
Renal hypoplasia, unilateral
Q60.4
Primary diagnosis candidate
Renal hypoplasia, bilateral
Q60.5
Primary diagnosis candidate
Renal hypoplasia, unspecified
Q60.6
Primary diagnosis candidate
Potter syndrome
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.
