Q61.5
BillableMedullary cystic kidney
Medullary cystic kidney
Status
Billable / Specific
Parent Code
Q61Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Nephronophthisis
- Sponge kidney NOS
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
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Congenital hepatic fibrosis79607001
- Muscle weakness of all four limbs91327001
- Quadriparesis91327001
- Tetraparesis91327001
- Medullary cystic disease204957003
- Medullary cystic disease of the kidney204957003
- Medullary cystic kidney204957003
- Medullary cystic kidney disease204957003
- Autosomal recessive medullary cystic disease204958008
- Familial juvenile medullary cystic kidney disease204958008
- Familial juvenile nephronophthisis204958008
- Nephronophthisis204958008
- Medullary sponge kidney236443009
- Nephronophthisis - medullary cystic disease253882001
- Medullary sponge kidney with nephrocalcinosis253884000
- Medullary sponge kidney without nephrocalcinosis253885004
- Fibrocystic kidney disease268234004
- Medullary cystic disease, adult type270910001
- Spastic quadriparesis298282001
- Spastic tetraparesis298282001
- Infantile nephronophthisis444558002
- Adolescent nephronophthisis444749006
- Juvenile nephronophthisis444830001
- Nephronophthisis type 4446989009
- Nephronophthisis type 5446991001
- Nephronophthisis type 6447335007
- Boichis disease717187000
- Boichis syndrome717187000
- Nephronophthisis hepatic fibrosis syndrome717187000
- Bilateral medullary sponge kidney717748005
- Medullary sponge kidney, bilateral717748005
- Autosomal dominant medullary cystic kidney disease with hyperuricaemia723373006
- Autosomal dominant medullary cystic kidney disease with hyperuricemia723373006
- Medullary cystic kidney disease 2723373006
- UMOD-related autosomal dominant tubulointerstitial kidney disease723373006
- Uromodulin related autosomal dominant tubulointerstitial kidney disease723373006
- RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia) syndrome723999009
- RHYNS syndrome723999009
- Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome723999009
- Autosomal dominant medullary cystic kidney disease without hyperuricaemia726017001
- Autosomal dominant medullary cystic kidney disease without hyperuricemia726017001
- MUC1-related autosomal dominant tubulointerstitial kidney disease726017001
- Medullary cystic kidney disease 1726017001
- Mucin 1 related autosomal dominant tubulointerstitial kidney disease726017001
- Autosomal dominant medullary cystic kidney disease726018006
- Autosomal dominant tubulointerstitial kidney disease726018006
- Adult familial nephronophthisis with spastic quadriparesia syndrome733650000
- Bilateral weakness of legs691011000124106
- Weakness of bilateral lower extremities691011000124106
- Weakness of bilateral lower limb691011000124106
- Weakness of both legs691011000124106
- Weakness of both lower extremities691011000124106
- Weakness of both lower limbs691011000124106
- Paresis of left lower extremity16018391000119104
- Paresis of left lower limb16018391000119104
- Paresis of right lower extremity16018431000119109
- Paresis of right lower limb16018431000119109
- Weakness of left leg570941000124100
- Weakness of left lower limb570941000124100
- Weakness of left upper limb570921000124107
- weakness of left arm570921000124107
- Weakness of right arm570961000124101
- Weakness of right upper limb570961000124101
- Weakness of right leg570971000124108
- Weakness of right lower limb570971000124108
UMLS
- Autosomal recessive medullary cystic diseaseC0687120
- Medullary cystic diseaseC0687120
- NPHC0687120
- NPHPC0687120
- NephronophthisisC0687120
- Nephronophthisis (disorder)C0687120
- cystic disease medullaryC0687120
- cystic kidneys medullaryC0687120
- juvenile nephronophthisisC0687120
- medullary cystic diseaseC0687120
- medullary cystic kidneyC0687120
- medullary cystic kidney diseaseC0687120
- nephronophthisisC0687120
- nephronopthisisC0687120
- Cacchi Ricci DiseaseC0022681
- Cacchi Ricci SyndromeC0022681
- Cacchi-Ricci SyndromeC0022681
- Cacchi-Ricci diseaseC0022681
- Canalicular Ectasia, PrecalycealC0022681
- Canalicular Ectasias, PrecalycealC0022681
- Disease, Cacchi RicciC0022681
- Ectasia, Precalyceal CanalicularC0022681
- Ectasias, Precalyceal CanalicularC0022681
- Kidney, SpongeC0022681
- Kidneys, SpongeC0022681
- Medullary Sponge KidneyC0022681
- Medullary Sponge KidneysC0022681
- Medullary sponge kidneyC0022681
- Medullary sponge kidney (disorder)C0022681
- Precalyceal Canalicular EctasiaC0022681
- Precalyceal Canalicular EctasiasC0022681
- Ricci Disease, CacchiC0022681
- Sponge KidneyC0022681
- Sponge Kidney, MedullaryC0022681
- Sponge KidneysC0022681
- Sponge Kidneys, MedullaryC0022681
- Sponge kidney NOSC0022681
- Sponge kidneysC0022681
- Syndrome, Cacchi-RicciC0022681
- kidney medullary spongeC0022681
- kidney spongeC0022681
- kidney sponge medullaryC0022681
- kidneys medullary spongeC0022681
- medullary sponge kidneyC0022681
- sponge kidneyC0022681
- sponge kidneysC0022681
- Medullary cystic disease (disorder)C2939174
- Medullary cystic disease of the kidneyC2939174
- Medullary cystic kidneyC2939174
- Medullary cystic kidney diseaseC2939174
Frequently Asked Questions
What is the ICD-10 code for medullary cystic kidney?
The ICD-10-CM code for medullary cystic kidney is Q61.5. The full clinical description is "Medullary cystic kidney". Q61.5 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q61.5 mean?
ICD-10-CM code Q61.5 represents "Medullary cystic 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 Q61.5 a billable code?
Yes, Q61.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q61.5 in?
Q61.5 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q61.5?
Q61.5 has Excludes1 notes indicating codes that cannot be used together with it, including: acquired cyst of kidney (N28.1); Potter's syndrome (Q60.6).
What SNOMED CT codes does Q61.5 map to?
Q61.5 maps to 31 SNOMED CT concepts: 444749006, 733650000, 726018006, 723373006, 726017001, and 26 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q61.5?
Q61.5 is linked to 3 UMLS Concept Unique Identifiers: C0687120, C0022681, C2939174. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.