Congenital renal dysplasia NOS
Multicystic Dysplastic Kidney
Multicystic Renal Dysplasias
Conorenal syndrome
Congenital absence of the kidney
Cystic renal dysplasia
Multicystic kidney disease
dysplastic kidneys
Dysplasia, Multicystic Renal
dysplasia kidney
Right kidney absent
dysplasia renal
Saldino-Mainzer dysplasia
Familial juvenile nephronophthisis
Renal Dysplasias, Multicystic
Autosomal recessive medullary cystic disease
Secondary renal dysplasia
Multicystic renal dysplasia, bilateral
Cirrhosis of pancreas
Dysplasias, Multicystic Renal
multicystic dysplastic kidneys
Familial juvenile medullary cystic kidney disease
Multiple renal cysts
Multicystic kidneys
Ulbright Hodes syndrome
MCKD - Multicystic kidney disease
Right renal agenesis
Multicystic renal dysplasia (disorder)
multicystic kidney dysplasia
Fibrosis of pancreas
Unilateral MCKD (multicystic kidney disease)
Multicystic kidney
Cystic dysplasia of kidney
Dysplastic kidney
Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome
Renal dysplasia and retinal aplasia
BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome
Hydranencephaly
Torticollis, keloids, cryptorchidism, renal dysplasia syndrome
Dysplasias, Multicystic Kidney
Ivemark II syndrome
dysplasia kidneys
Left kidney absent
Thymic-renal-anal-lung dysplasia
Agenesis of right kidney co-occurrent with congenital dysplasia of left kidney
Renal hepatic pancreatic dysplasia
Renal dysplasia (disorder)
Bilateral renal dysplasia
Bilateral secondary renal dysplasia
Renal dysplasia due to foetal exposure to angiotensin converting enzyme inhibitor
multicystic renal dysplasia
Loken Senior syndrome
Nephronophthisis
Secondary renal dysplasia, bilateral
Thymic, renal, anal, lung dysplasia syndrome
Renal Dysplasia, Multicystic
Left renal agenesis co-occurrent with right renal dysplasia
Agenesis of right kidney
Bilateral renal dysgenesis
Dysplasia of kidney
Dysplasia of left kidney
Agenesis of left kidney co-occurrent with dysplasia of right kidney
X-linked mental retardation Reish type
Bilateral multicystic renal dysplasia
Primary renal dysplasia
Unilateral multicystic renal dysplasia
Renal dysplasia due to fetal exposure to angiotensin converting enzyme inhibitor
Congenital absence of cerebral hemispheres
BRESEK syndrome
Dysplasia of right kidney
Retinal pigment epithelial dystrophy
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome
Agenesis of left kidney
Agenesis of right kidney co-occurrent with dysplasia of left kidney
Agenesis of left kidney co-occurrent with congenital dysplasia of right kidney
Left renal agenesis
Kidney Dysplasias, Multicystic
Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome
Renal agenesis
Multicystic Kidney Dysplasias
Kidney Dysplasia, Multicystic
Renohepaticopancreatic dysplasia
Dysplasia, Multicystic Kidney
MARCH syndrome
kidney dysplasia
Congenital renal dysplasia
Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome
Multicystic kidney (development)
Renal dysplasia, mesomelia, radiohumeral fusion syndrome
Right renal agenesis co-occurrent with left renal dysplasia
Primitive renal tubule syndrome
Renal dysplasia with limb defect syndrome

Frequently Asked Questions

What is the ICD-10 code for renal dysplasia?

The ICD-10-CM code for renal dysplasia is Q61.4. The full clinical description is "Renal dysplasia". Q61.4 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q61.4 mean?

ICD-10-CM code Q61.4 represents “Renal dysplasia”. 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 Q61.4 a billable code?

Yes, Q61.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q61.4 in?

Q61.4 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q61.4?

Q61.4 has Excludes1 notes indicating codes that cannot be used together with it, including: acquired cyst of kidney (N28.1); Potter's syndrome (Q60.6); polycystic kidney disease (Q61.11-Q61.3).

What SNOMED CT codes does Q61.4 map to?

Q61.4 maps to 32 SNOMED CT concepts: 762907005, 762912006, 762908000, 762911004, 204958008, and 27 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q61.4?

Q61.4 is linked to 4 UMLS Concept Unique Identifiers: C3536714, C3714581, C2910226, C2910227. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q61.4 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like renal dysplasia 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 Q61.4?

Q61.4 maps to the ICD-11 code: LB30.1 (Renal dysplasia).

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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.