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Definition
ICD-10-CM
Code
Q61.2
Polycystic kidney, adult type
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Hierarchy
Q00-Q99
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Q60-Q64
Congenital malformations of the urinary system (Q60-Q64)
Q61
Cystic kidney disease
Q61.0
Congenital renal cyst
Q61.1
Polycystic kidney, infantile type
Q61.2
Polycystic kidney, adult type
Q61.3
Polycystic kidney, unspecified
Q61.4
Renal dysplasia
Q61.5
Medullary cystic kidney
Q61.8
Other cystic kidney diseases
Q61.9
Cystic kidney disease, unspecified
Notes
Q00-Q99
Codes from this chapter are not for use on maternal records
Inclusion Terms
Q61.2
Polycystic kidney, autosomal dominant
Excludes 1
Q61
acquired cyst of kidney (N28.1)
N28.1
Cyst of kidney, acquired
Q60.6
Potter's syndrome
Excludes 2
Q00-Q99
inborn errors of metabolism (E70-E88)
E70-E88
Metabolic disorders (E70-E88)
Related Terms
Cyst (colloid) (mucous) (simple) (retention) congenital NEC kidney more than one (multiple) specified as polycystic adult type
Cyst (colloid) (mucous) (simple) (retention) kidney more than one (multiple) specified as polycystic adult type (autosomal dominant)
Cystic kidney (congenital) adult type
Degeneration, degenerative kidney polycystic adult type (autosomal dominant)
Disease, diseased kidney (functional) (pelvis) polycystic adult type
Disease, diseased polycystic kidney or renal adult type
Disease, diseased renal (functional) (pelvis) polycystic (congenital) adult type
Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic) polycystic adult type
Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic) polycystic autosomal dominant
Polycystic (disease) degeneration, kidney autosomal dominant (adult type)
Polycystic (disease) kidney autosomal dominant
Polycystic (disease) kidney autosomal dominant (adult type)