Ad
related to: icd 10 kidney mass unspecified
Search results
Results From The WOW.Com Content Network
584.9 Renal failure, acute, unspec. 585 Chronic renal failure; 586 Renal failure, unspecified; 587 Renal sclerosis, unspecified; 588 Disorders resulting from impaired renal function. 588.8 Other specified disorders resulting from impaired renal function. 588.81 Hyperparathyroidism, secondary, renal; 588.89 Renal tubular acidosis; 589 Small ...
Renal hypoplasia is a congenital abnormality in which one or both of the kidneys are smaller than normal, [5] resulting in a reduced nephron number [1] but with normal morphology.
This is a shortened version of the second chapter of the ICD-9: Neoplasms. It covers ICD codes 140 to 239. The full chapter can be found on pages 101 to 144 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.
The RENAL Nephrometry Scoring System is used to measure the complexity of kidney tumors for determining whether a renal mass is appropriate for partial or radical nephrectomy, and is estimated by CT scan as follows: [7] The nephrometery score takes into account the size of the tumor (Radius), how much of the tumor is inside or outside of the ...
The ICD-10 Procedure Coding System (ICD-10-PCS) is a US system of medical classification used for procedural coding.The Centers for Medicare and Medicaid Services, the agency responsible for maintaining the inpatient procedure code set in the U.S., contracted with 3M Health Information Systems in 1995 to design and then develop a procedure classification system to replace Volume 3 of ICD-9-CM.
This is a shortened version of the fourteenth chapter of the ICD-9: Congenital Anomalies. It covers ICD codes 740 to 759. The full chapter can be found on pages 417 to 437 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.
Cystic kidney disease includes various conditions related to the formation of cysts in one or both kidneys. The most common subset is polycystic kidney disease (PKD), which is a genetic anomaly with two subsets, autosomal recessive polycystic kidney disease (ARPKD) and autosomal dominant polycystic kidney disease (ADPKD).
A cystic nephroma, also known as multilocular cystic nephroma, mixed epithelial stromal tumour (MEST) and renal epithelial stromal tumour (REST), [1] is a type of rare benign kidney tumour. Symptoms [ edit ]