
2015 ICD-9-CM Diagnosis Code 753.12
Polycystic kidney, unspecified type
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- ICD-9-CM 753.12 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 753.12 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:
753.12 converts directly to:
- 2015/16 ICD-10-CM Q61.3 Polycystic kidney, unspecified
Approximate Synonyms
- Congenital cystic kidney disease
- Polycystic kidney disease
Clinical Information
- A usually autosomal dominant and less frequently autosomal recessive genetic disorder characterized by the presence of numerous cysts in the kidneys leading to end-stage renal failure. The autosomal dominant trait is associated with abnormalities on the short arm of chromosome 16. Symptoms in patients with the autosomal dominant trait usually appear at middle age and include abdominal pain, hematuria, and high blood pressure. Patients may develop brain aneurysms and liver cysts. Patients with the autosomal recessive trait present with progressive renal failure early in life and symptoms resulting from hepatic fibrosis. The autosomal recessive trait is associated with abnormalities of chromosome 6. Polycystic kidney disease may also result as a side effect in patients on renal dialysis
- Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed cysts within the kidney; there is an autosomal recessive form appearing in childhood and a later appearing autosomal dominant form; a similar acquired disease sometimes accompanies end-stage renal disease
- Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed cysts within the kidneys. They include diseases with autosomal dominant and autosomal recessive inheritance
ICD-9-CM Volume 2 Index entries containing back-references to
753.12:
- Degeneration, degenerative
kidney (see also Sclerosis, renal) 587
renal (see also Sclerosis, renal) 587

fibrocystic 753.19

polycystic 753.12
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
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
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
- Polycystic (congenital) (disease) 759.89

kidney (congenital) 753.12