Cyst of kidney, acquired. 2016 2017 2018 2019 2020 2021 Billable/Specific Code. N28.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2021 edition of ICD-10-CM N28.1 became effective on October 1, 2020.
ICD-9-CM 593.2 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 593.2 should only be used for claims with a date of service on or before September 30, 2015.
Short description: Liver disorders NEC. ICD-9-CM 573.8 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 573.8 should only be used for claims with a date of service on or before September 30, 2015.
N28- Other disorders of kidney and ureter, not elsewhere classified N28.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM N28.1 became effective on October 1, 2019.
N99. 520 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM N99. 520 became effective on October 1, 2021.
ICD-10 code N28. 1 for Cyst of kidney, acquired is a medical classification as listed by WHO under the range - Diseases of the genitourinary system .
ICD-10-CM Code for Polycystic kidney, adult type Q61. 2.
N28. 1 - Cyst of kidney, acquired | ICD-10-CM.
N28. 1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
(Congenital Renal Cystic Dysplasia) Congenital cystic dysplasia of the kidneys is a broad category of birth defects involving the kidneys and/or urinary tract that may cause blockage of the flow of urine. Congenital cystic dysplasia affects one or both kidneys.
A multicystic dysplastic kidney (MCDK) is the result of abnormal fetal development of the kidney. The kidney consists of irregular cysts of varying sizes that resemble a bunch of grapes. A multicystic dysplastic kidney has no function and nothing can be done to save it.
Autosomal recessive polycystic kidney disease (ARPKD) is a rare inherited childhood condition where the development of the kidneys and liver is abnormal. Over time, either one of these organs may fail.