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Q63.8

Billable

Other specified congenital malformations of kidney

Other specified congenital malformations of kidney

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Congenital renal calculi

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(5)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(115)

SNOMED CT

Clinical Terms

  • Congenital calculus of kidney
  • Diverticulum of renal calyx
  • Congenital primary hydronephrosis, bilateral
  • Trifid pelvis of kidney
  • Dilatation of calyx without dilatation of pelvis and ureter
  • Dilatation of renal pelvis
  • Congenital asymmetry of kidneys
  • Bilateral hydronephrosis
  • Congenital megacalycosis of both kidneys
  • Pyelectasis
  • Congenital pyelectasia
  • Pyelectasia
  • Calyceal dilatation
  • Congenital dilation of renal pelvis
  • Congenital misshapen kidney
  • Megacalycosis
  • Accessory kidney
  • Congenital hydronephrosis
  • Prominent renal pelvis
  • Infundibulopelvic stenosis multicystic kidney syndrome
  • Congenital calculus of kidney (disorder)
  • Trifid kidney
  • Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes
  • Diffuse hyperplastic perilobular nephroblastomatosis
  • Infundibulopelvic dysgenesis
  • Congenital renal calculus
  • DHPLN - diffuse hyperplastic perilobular nephroblastomatosis
  • Congenital hydrocalicosis
  • Diffuse perilobar nephrogenic rests
  • Congenital megacalycosis
  • Congenital megacalycosis of bilateral kidneys
  • PELVIS (Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome
  • Renal asymmetry
  • Triple kidney with triple pelvis
  • Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunisation
  • Congenital renal calculi
  • Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome
  • Congenital calyceal diverticulum
  • Dilation of renal pelvis
  • Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
  • PELVIS (perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome
  • Calicectasis
  • Primary hydronephrosis
  • Nodular renal blastema
  • Bilateral congenital primary hydronephrosis
  • Congenital abnormal shape of kidney
  • Dilation of calyx
  • Congenital dilatation of renal pelvis
  • Caliectasis
  • Renal caliceal diverticuli and deafness syndrome
  • PELVIS syndrome
  • Dilatation of calyx
  • Supernumerary kidney
  • Inequality in size of kidneys
  • Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome
  • Calyceal diverticulum
Frequently Asked Questions
What is the ICD-10 code for other specified congenital malformations of kidney?

The ICD-10-CM code for other specified congenital malformations of kidney is Q63.8. The full clinical description is "Other specified congenital malformations of kidney". Q63.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q63.8 mean?

ICD-10-CM code Q63.8 represents “Other specified congenital malformations of kidney”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q63.8 a billable code?

Yes, Q63.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q63.8 in?

Q63.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q63.8?

Q63.8 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital nephrotic syndrome (N04.-).

What SNOMED CT codes does Q63.8 map to?

Q63.8 maps to 28 SNOMED CT concepts: 30275001, 237610008, 717750002, 95581005, 371011007, and 23 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q63.8?

Q63.8 is linked to 2 UMLS Concept Unique Identifiers: C0266300, C0478058. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q63.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified congenital malformations of kidney affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q63.8?

Q63.8 maps to the ICD-11 code: LB30.Z (Structural developmental anomalies of kidneys, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.