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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Congenital Anomalies Of Urinary System 753.* > 2007 ICD-9-CM Diagnosis 753.19 Other specified cystic kidney disease This code may be outdated. View the most recent version of ICD-9-CM 753.19 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