2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Congenital Anomalies Of Urinary System 753.* > 2006 ICD-9-CM Diagnosis 753.14 Polycystic kidney autosomal recessive View the most recent version of ICD-9-CM 753.14 A rare genetic disorder with autosomal recessive inheritance characterized by multiple cysts in both kidneys and associated hepatic lesions. Serious manifestations are usually present at birth and there is high perinatal mortality. 753.14 is a specific code that can be used to specify a diagnosis 753.14 contains 21 index entries View the ICD-9-CM Volume 1 753.* hierarchy  Index entries containing 753.14: Degeneration, degenerative kidney (see also Sclerosis, renal) 587 polycystic (congenital) 753.12 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 renal (see also Sclerosis, renal) 587 polycystic 753.12 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 Disease, diseased - see also Syndrome kidney (functional) (pelvis) (see also Disease, renal) 593.9 polycystic (congenital) 753.12 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 polycystic (congenital) 759.89 kidney or renal 753.12 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 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 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14 Polycystic (congenital) (disease) 759.89 kidney (congenital) 753.12 autosomal recessive 753.14 childhood type (CPKD) 753.14 infantile type 753.14