ICD-10-CM Codes Q00-Q99 Q60-Q64 Q61 Q61.19

ICD-10-CM Diagnosis Code Q61.19

Effective Date: 10/01/2015 To 09/30/2025

Other polycystic kidney, infantile type

CMS-HCC-V24	CMS-HCC-V28	RxHCC	Age	Gender	Maternity	Acute or Chronic	MCC
--	--	--	--	--	--	Acute	No

Back-references to Q61.19

Cyst(colloid) (mucous) (simple) (retention)

congenital NEC Q89.8
- kidney Q61.00
  - more than one(multiple) Q61.02
    - specified as polycystic Q61.3
      - infantile type NEC Q61.19
kidney N28.1
- more than one(multiple) Q61.02
  - specified as polycystic Q61.3
    - infantile type(autosomal recessive) NEC Q61.19

Cystic see also condition

Degeneration, degenerative

kidney N28.89
- polycystic Q61.3
  - infantile type(autosomal recessive) NEC Q61.19

Disease, diseased see also Syndrome

kidney(functional) (pelvis) N28.9
- polycystic Q61.3
  - childhood type NEC Q61.19
polycystic
- kidney or renal Q61.3
  - childhood type NEC Q61.19
renal(functional) (pelvis) see also Disease, kidney N28.9
- polycystic(congenital) Q61.3
  - childhood type NEC Q61.19

polycystic Q61.3
- autosomal
  - recessive NEC Q61.19
- childhood type NEC Q61.19
- infantile type NEC Q61.19

Polycystic(disease)

degeneration, kidney Q61.3
- autosomal recessive(infantile type) NEC Q61.19
kidney Q61.3
- autosomal
  - recessive NEC Q61.19
- autosomal recessive(childhood type) NEC Q61.19
- infantile type NEC Q61.19

Chapter, Section and Diagnosis Prefix for Q61.19