Q63 refers to Other congenital malformations of kidney, a category covering congenital abnormalities affecting the kidneys, renal pelvis, ureters, or urinary tract system detected prenatally or after birth.

Symptoms

Absent kidney – Seen in renal agenesis (Q60)
Fluid-filled cysts – Typical of cystic kidney disease (Q61)
Urinary tract obstruction – Seen in renal pelvis/ureter defects (Q62)
Recurrent urinary infections – Often a complication of malformations (Q63–Q64)
Swelling of abdomen – From fluid buildup due to obstructive defects

Diagnosis

Diagnosis often involves prenatal ultrasound screening, postnatal renal ultrasounds, voiding cystourethrograms (VCUG), MRI scans, and sometimes genetic testing to identify congenital anomalies of the kidney and urinary tract.

ICD10 Code Usage

ICD10 code Q63 is critical for documenting congenital kidney or urinary malformations in medical records, insurance coding, surgical referrals, and long-term renal management planning.

Related Codes

FAQs

Q1: What is ICD10 code Q63?
A: It documents Other congenital malformations of kidney, covering congenital abnormalities of the kidneys, ureters, or urinary system.

Q2: Can kidney agenesis (Q60) be fatal?
A: Bilateral renal agenesis (no kidneys) is typically fatal without intervention; unilateral cases may live normal lives.

Q3: How is cystic kidney disease managed?
A: It depends on severity but may involve monitoring, blood pressure control, and sometimes surgical interventions.

Q4: Are obstructive urinary defects always symptomatic?
A: Some cause early symptoms (e.g., hydronephrosis), while others are discovered incidentally.

Q5: Can these defects be corrected surgically?
A: Yes, many obstructive and anatomical issues can be surgically corrected to preserve kidney function.

Conclusion

ICD10 code Q63 ensures accurate documentation of Other congenital malformations of kidney, aiding early diagnosis, appropriate intervention, and better outcomes for individuals with congenital kidney and urinary tract malformations.