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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Congential Anomalies 740-759 > Congenital Anomalies Of Urinary System 753.* > 2008 ICD-9-CM Diagnosis 753.19 Other specified cystic kidney disease  On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date. The 2009 version of ICD-9-CM 753.19 can be accessed here. A severe form of dysplasia where the kidney typically appears as a bunch of grapes without a reniform configuration or calyceal drainage system. It occurs in-utero and is the most common form of nongenetic renal cystic disease. 753.19 is a specific code that can be used to specify a diagnosis 753.19 contains 15 index entries View the ICD-9-CM Volume 1 753.* hierarchy 753.19 also known as: Multicystic kidney Index entries containing 753.19: Cyst (mucus) (retention) (serous) (simple) congenital NEC 759.89 kidney 753.10 multiple 753.19 kidney (congenital) 753.10 multiple 753.19 Cystic - see also condition disease kidney, congenital 753.10 multiple 753.19 specified NEC 753.19 kidney, congenital 753.10 multiple 753.19 specified NEC 753.19 Degeneration, degenerative kidney (see also Sclerosis, renal) 587 fibrocystic (congenital) 753.19 renal (see also Sclerosis, renal) 587 fibrocystic 753.19 Disease, diseased - see also Syndrome kidney (functional) (pelvis) (see also Disease, renal) 593.9 cystic (congenital) 753.10 multiple 753.19 specified NEC 753.19 fibrocystic (congenital) 753.19 renal (functional) (pelvis) (see also Disease, kidney) 593.9 fibrocystic (congenital) 753.19 Fibrocystic disease 277.00 kidney (congenital) 753.19 kidney (congenital) 753.19 Multicystic kidney 753.19