Q61.19 – Other polycystic kidney, infantile type
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
GEM Conversion to ICD-9 CM
Fs: 10000
–
Polycystic kidney, autosomal recessive
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
infantile type NEC
(autosomal recessive)
Q61.19
Cystic
See also condition
Degeneration, degenerative
infantile type NEC
(autosomal recessive)
Q61.19
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 recessive NEC
(infantile type)
Q61.19
autosomal
autosomal recessive NEC
(childhood type)
Q61.19
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 |
| Q61.1 | Polycystic kidney, infantile type |
| Q61.19 | Other polycystic kidney, infantile type |