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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 753.13 Polycystic kidney autosomal dominant A genetic disorder with autosomal dominant inheritance characterized by multiple cysts in both kidneys and progressive deterioration of renal function. Type 1 is usually caused by a mutant gene at the PKD1 locus on the short arm of chromosome 16, though mutations elsewhere in the genome can also cause the disease. The age of onset of symptoms varies widely. 753.13 is a specific code that can be used to specify a diagnosis 753.13 contains 14 index entries View the ICD-9-CM Volume 1 753.* hierarchy Index entries containing 753.13: Degeneration, degenerative kidney (see also Sclerosis, renal) 587 polycystic (congenital) 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 renal (see also Sclerosis, renal) 587 polycystic 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 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 polycystic (congenital) 759.89 kidney or renal 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 renal (functional) (pelvis) (see also Disease, kidney) 593.9 polycystic (congenital) 753.12 adult type (APKD) 753.13 autosomal dominant 753.13 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 Polycystic (congenital) (disease) 759.89 kidney (congenital) 753.12 adult type (APKD) 753.13 autosomal dominant 753.13