Q61.2 Polycystic kidney, adult type

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

Applicable To

Polycystic kidney, autosomal dominant

GEM Conversion to ICD-9 CM


MDC / MS-DRG Reference


Back Reference of Diagnostic Codes

Cyst (colloid) (mucous) (simple) (retention)
more than one (multiple) Q61.02
kidney (acquired) N28.1
more than one (multiple) Q61.02
adult type (autosomal dominant) Q61.2
Cystic See also condition
kidney (congenital) Q61.9
Degeneration, degenerative
adult type (autosomal dominant) Q61.2
Disease, diseased See also Syndrome
kidney (functional) (pelvis) N28.9
polycystic
renal (functional) (pelvis) See also Disease, kidney N28.9
polycystic (congenital) Q61.3
Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic) N05.9
autosomal
Polycystic (disease)
autosomal dominant (adult type) Q61.2
autosomal
autosomal dominant (adult type) Q61.2

Sibling Codes


Parent Sibling Codes


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Code Title
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Q60-Q64 Congenital malformations of the urinary system (Q60-Q64)
Q61 Cystic kidney disease
Q61.2 Polycystic kidney, adult type
Applicable to
Polycystic kidney, autosomal dominant