Q63.8
BillableOther 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 mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(115)
SNOMED CT
- Congenital hydronephrosis16297002
- Primary hydronephrosis16297002
- Inequality in size of kidneys19167000
- Renal asymmetry19167000
- Accessory kidney30275001
- Supernumerary kidney30275001
- Congenital calculus of kidney48061001
- Congenital renal calculus48061001
- Trifid pelvis of kidney59758007
- Dilatation of calyx without dilatation of pelvis and ureter85901000
- Megacalycosis85901000
- Nodular renal blastema88102009
- Congenital abnormal shape of kidney92921005
- Congenital misshapen kidney92921005
- Bilateral hydronephrosis95581005
- Dilatation of renal pelvis197820003
- Dilation of renal pelvis197820003
- Pyelectasia197820003
- Pyelectasis197820003
- Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes237610008
- Trifid kidney253862000
- Congenital calyceal diverticulum253875000
- Triple kidney with triple pelvis270517006
- Congenital hydrocalicosis278531007
- Calicectasis371011007
- Caliectasis371011007
- Calyceal dilatation371011007
- Dilatation of calyx371011007
- Dilation of calyx371011007
- Calyceal diverticulum433036004
- Diverticulum of renal calyx433036004
- Prominent renal pelvis699055002
- Bilateral congenital primary hydronephrosis717750002
- Congenital primary hydronephrosis, bilateral717750002
- PELVIS (Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome725138002
- PELVIS (perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome725138002
- PELVIS syndrome725138002
- Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome725138002
- Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome725138002
- Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunisation725592009
- Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization725592009
- Infundibulopelvic dysgenesis725905005
- Infundibulopelvic stenosis multicystic kidney syndrome725905005
- Renal caliceal diverticuli and deafness syndrome782942003
- Congenital megacalycosis of bilateral kidneys890370003
- Congenital megacalycosis of both kidneys890370003
- Congenital megacalycosis1137561000
- DHPLN - diffuse hyperplastic perilobular nephroblastomatosis1306776003
- Diffuse hyperplastic perilobular nephroblastomatosis1306776003
- Diffuse perilobar nephrogenic rests1306776003
- Congenital asymmetry of kidneys288280591000119107
- Congenital dilatation of renal pelvis111631000119106
- Congenital dilation of renal pelvis111631000119106
- Congenital pyelectasia111631000119106
UMLS
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.