Abnormal kidneys
Acrorenal syndrome
Joubert syndrome
Congenital short fibula
Syndactyly, telecanthus, anogenital and renal malformation syndrome
Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
Congenital renal anomaly NOS
Atresia ani
Congenital vertebral, cardiac, renal anomalies syndrome
Neurofaciodigitorenal syndrome
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome
kidney malformations
Aproctia
Passwell Goodman Siprkowski syndrome
anomalies congenital renal
Familial juvenile nephronophthisis
abnormalities congenital kidney
Autosomal recessive medullary cystic disease
Saito Kuba Tsuruta syndrome
Congenital anomaly of kidney
Congenital hypoplasia of bone of radius and/or ulna
HLTRS (hypotrichosis, lymphoedema, telangiectasia, renal defect) syndrome
Familial aplasia of the vermis
Fibuloulnar hypoplasia with renal abnormalities
Cerebello-oculo-renal syndrome
Arima syndrome
Congenital anomaly of renal pelvis
STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome
SERKAL (sex reversion, kidney, adrenal and lung dysgenesis) syndrome
Renal anomaly
Familial juvenile medullary cystic kidney disease
STAR syndrome
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome
Joubert syndrome with oculorenal defect
Congenital anomaly of the kidney (disorder)
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome
anomalies congenital kidney
Congenital atresia of anus
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome
Congenital short ulna
VACTERL syndrome with hydrocephalus
SERKAL syndrome
Split hand and split foot with mandibular hypoplasia syndrome
Renal malformation
Thauvin Robinet Faivre syndrome
Acro-renal-mandibular syndrome
Fusion of kidneys
Telecanthus
Congenital anomaly of ureter and renal pelvis
Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
Renal malformations
Imperforate anus
Fibulo-ulnar hypoplasia and renal anomalies syndrome
Horseshoe kidney
Acrorenal mandibular syndrome
Congenital fusion of kidneys
Congenital abnormality of kidney
Nephronophthisis
Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-oesophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
Radio-renal syndrome
Eastman Bixler syndrome
anomalies renal
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome
Kidney malformation
Acro-renal-ocular syndrome
HLTRS (hypotrichosis, lymphedema, telangiectasia, renal defect) syndrome
Congenital hypoplasia of fibula
Abnormal kidney
Congenital imperforate anus
Kidney abnormalities
Acrorenoocular syndrome
Mitochondrial DNA depletion syndrome hepatocerebrorenal form
Cardiomyopathy and renal anomaly syndrome
Congenital hypoplasia of ulna
Hypotrichosis, lymphoedema, telangiectasia, renal defect syndrome
Tall stature, intellectual disability, renal anomalies syndrome
Faciocardiorenal syndrome
Congenital NAD deficiency disorder
Freire Maia Pinheiro Opitz syndrome
Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form
Congenital anomaly of the kidney
Defect of vertebral segmentation
Sex reversion, kidney, adrenal and lung dysgenesis syndrome
NFDR (neurofaciodigitorenal) syndrome
Anal atresia
Congenital hypoplasia of bone of forearm
Abnormality of the kidney
Renal anomalies
VACTERL syndrome

Frequently Asked Questions

What is the ICD-10 code for congenital malformation of kidney, unspecified?

The ICD-10-CM code for congenital malformation of kidney, unspecified is Q63.9. The full clinical description is "Congenital malformation of kidney, unspecified". Q63.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q63.9 mean?

ICD-10-CM code Q63.9 represents “Congenital malformation of kidney, unspecified”. 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 Q63.9 a billable code?

Yes, Q63.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q63.9 in?

Q63.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q63.9?

Q63.9 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital nephrotic syndrome (N04.-).

What SNOMED CT codes does Q63.9 map to?

Q63.9 maps to 32 SNOMED CT concepts: 720414005, 720415006, 720458005, 204712000, 721862000, and 27 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q63.9?

Q63.9 is linked to 1 UMLS Concept Unique Identifier: C0266292. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q63.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of kidney, unspecified 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 Q63.9?

Q63.9 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.