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
Fs: 00000
–
Polycystic kidney, autosomal dominant
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
Cyst
(colloid) (mucous) (simple) (retention)
more than one
(multiple)
Q61.02
more than one
(multiple)
Q61.02
adult type
(autosomal dominant)
Q61.2
Cystic
See also condition
Degeneration, degenerative
adult type
(autosomal dominant)
Q61.2
Disease, diseased
See also Syndrome
polycystic
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
View in Tabular
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
|