2015 ICD-9-CM Diagnosis Code 753.13
Polycystic kidney, autosomal dominant
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- ICD-9-CM 753.13 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 753.13 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
Convert to ICD-10-CM:
753.13 converts directly to:
- 2015/16 ICD-10-CM Q61.2 Polycystic kidney, adult type
Approximate Synonyms
- Autosomal dominant adult polycystic kidney disease
- Polycystic kidney disease, adult type
- Polycystic kidney, adult type
Clinical Information
- Kidney disorders with autosomal dominant inheritance and characterized by multiple cysts in both kidneys with progressive deterioration of renal function
- Polycystic kidney disease inherited in an autosomal dominant pattern. Symptoms usually appear at middle age and include abdominal pain, hematuria and high blood pressure. Patients may develop brain aneurysms and liver cysts
ICD-9-CM Volume 2 Index entries containing back-references to
753.13:
- Degeneration, degenerative
- kidney (see also Sclerosis, renal) 587
- renal (see also Sclerosis, renal) 587
- fibrocystic 753.19
- polycystic 753.12
- adult type (APKD) 753.13
- autosomal dominant 753.13
- autosomal recessive 753.14
- childhood type (CPKD) 753.14
- Disease, diseased - see also Syndrome
- kidney (functional) (pelvis) (see also Disease, renal) 593.9
- chronic 585.9
- requiring chronic dialysis 585.6
- stage
- cystic (congenital) 753.10
- fibrocystic (congenital) 753.19
- in gout 274.10
- 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
- renal (functional) (pelvis) (see also Disease, kidney) 593.9
- with
- edema (see also Nephrosis) 581.9
- exudative nephritis 583.89
- lesion of interstitial nephritis 583.89
- stated generalized cause - see Nephritis
- acute 593.9
- basement membrane NEC 583.89
- with pulmonary hemorrhage (Goodpasture's syndrome) 446.21 [583.81]
- chronic (see also Disease, kidney, chronic) 585.9
- complicating pregnancy or puerperium NEC 646.2
- with hypertension - see Toxemia, of pregnancy
- affecting fetus or newborn 760.1
- cystic, congenital (see also Cystic, disease, kidney) 753.10
- diabetic 250.4 [583.81]
- due to
- end-stage 585.6
- exudative 583.89
- fibrocystic (congenital) 753.19
- gonococcal 098.19 [583.81]
- gouty 274.10
- hypertensive (see also Hypertension, kidney) 403.90
- immune complex NEC 583.89
- interstitial (diffuse) (focal) 583.89
- lupus 710.0 [583.81]
- maternal, affecting fetus or newborn 760.1
- phosphate-losing (tubular) 588.0
- 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
- specified lesion or cause NEC (see also Glomerulonephritis) 583.89
- subacute 581.9
- syphilitic 095.4
- tuberculous (see also Tuberculosis) 016.0 [583.81]
- tubular (see also Nephrosis, tubular) 584.5
- 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