Q61.19
Other polycystic kidney, infantile type
Billable code
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Inherited from Q61.1Polycystic kidney, infantile type
Synonyms
Polycystic kidney, autosomal recessive
Inherited from Q61Cystic kidney disease
Inherited from chapter 17Congenital malformations, deformations and chromosomal abnormalities
Excludes 2
inborn errors of metabolism (E70-E88)
Note
Codes from this chapter are not for use on maternal records
Official Guidelines for Q61.19
FY 2026 ›Sections that reference Q61.19
Sections whose FY 2026 text names Q61.19, its Q61 category, or a range containing it — the chapter guidance above is the authoritative source.
Find Q61.19 in the alphabetic index
14 index paths lead to this code
- Cystic › kidney › infantile type NEC
- Nephritis, nephritic › polycystic › childhood type NEC
- Nephritis, nephritic › polycystic › infantile type NEC
- Polycystic › degeneration, kidney › autosomal recessive NEC
- Polycystic › kidney › autosomal recessive NEC
- Polycystic › kidney › infantile type NEC
- Degeneration, degenerative › kidney › polycystic › infantile type NEC
- Disease, diseased › kidney › polycystic › childhood type NEC
- Disease, diseased › polycystic › kidney or renal › childhood type NEC
- Disease, diseased › renal › polycystic › childhood type NEC
- Nephritis, nephritic › polycystic › autosomal › recessive NEC
- Polycystic › kidney › autosomal › recessive NEC
- Cyst › kidney › more than one › specified as polycystic › infantile type NEC
- Cyst › congenital NEC › kidney › more than one › specified as polycystic › infantile type NEC