2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Congenital Anomalies Of Urinary System 753.* > 2006 ICD-9-CM Diagnosis 753.12 Polycystic kidney unspecified type View the most recent version of ICD-9-CM 753.12 Diseases that are characterized by the progressive expansion of a large number of tightly packed cysts within the kidney. 753.12 is a specific code that can be used to specify a diagnosis 753.12 contains 7 index entries View the ICD-9-CM Volume 1 753.* hierarchy  Index entries containing 753.12: Degeneration, degenerative kidney (see also Sclerosis, renal) 587 polycystic (congenital) 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 renal (see also Sclerosis, renal) 587 polycystic 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 autosomal recessive 753.14 Disease, diseased - see also Syndrome kidney (functional) (pelvis) (see also Disease, renal) 593.9 polycystic (congenital) 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 polycystic (congenital) 759.89 kidney or renal 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 renal (functional) (pelvis) (see also Disease, kidney) 593.9 polycystic (congenital) 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 Nephritis, nephritic (albuminuric) (azotemic) (congenital) (degenerative) (diffuse) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic) 583.9 polycystic 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 Polycystic (congenital) (disease) 759.89 kidney (congenital) 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14