Q60.5 ICD-10-CM Code: Renal hypoplasia, unspecified
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 3 inclusion terms
Inpatient Payment Groups (MS-DRG)
Potential MS-DRG participation — not a DRG assignment.
MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v43, Appendix B.
- MS-DRG 698 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH MCC (MDC 11)
- MS-DRG 699 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH CC (MDC 11)
- MS-DRG 700 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITHOUT CC/MCC (MDC 11)
A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for Q60.5 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on Q60.5 itself; “inherited from” names the category or block whose note applies here.
Includes
Conditions the official ICD-10-CM tabular list includes under this code.
- congenital absence of kidney
- congenital atrophy of kidney
- infantile atrophy of kidney
Source: inherited from Q60
Coder workflow for Q60.5
MedCoder structured workflow — derived from this code’s own official record
Before you code Q60.5
- Unspecified does not mean incorrect. When the record gives no greater specificity, Q60.5 may be the appropriate code. Check the record for detail that supports a more specific sibling. An unspecified code is for records that do not provide the detail a more specific code needs; a query, not an assumption, is the route to specificity (Guidelines I.A.9.b, I.B.18).
ReviewQ60.0, Q60.1, Q60.3, Q60.4, Q60.6
See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →
- Laterality is coded in this family. Confirm the side documented — right, left, or bilateral — and select the matching code (this page’s code: unspecified). The unspecified-side code applies only when the record states no side. Laterality is assigned from the documented side; where a bilateral code exists and both sides are documented, it is used instead of two unilateral codes (Guidelines I.B.13).
ReviewQ60.4 · bilateral
Choose the right path
- Does the record document the detail a more specific sibling code needs?
Yes → Review the specific siblings in this subcategory.
No → Continue — Q60.5 is appropriate when the documentation goes no further. - Is the side documented?
Yes → Select the code for the documented side (or the bilateral code when both sides are documented and one exists).
No → Use the unspecified-side code only when the record states no side; a query is the alternative.ReviewQ60.4 · bilateral
Consider Q60.5. Then confirm the code is valid for the date of service in the Verify section.
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
- Laterality
- Right, left or bilateral as documented; unspecified only when the record states no side (Guidelines I.B.13).
- Any detail beyond this code’s title
- What the record states that a more specific sibling code would capture — or its absence, which itself supports the unspecified code.
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: The provider documents the condition in the terms of this code’s title and records no further detail.
Coding question: Is a more specific sibling code supportable?
Path: Review the specific siblings in this subcategory and what each requires the record to state.
Reason: A more specific code needs documentation of the distinguishing element; without it the unspecified code is appropriate, and a provider query is the route to specificity (Guidelines I.A.9.b, I.B.18).
Documentation: The record documents the condition on one side only.
Coding question: Which code in this family applies?
Path: Select the sibling code for the documented side.
Reason: Laterality is assigned from the documented side; the unspecified-side code is for records that state no side (Guidelines I.B.13).
ReviewQ60.4 · bilateral
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Indexed Clinical Terms (3)
Official source data — entries quoted as published, in the Index’s own lookup phrasing
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.
Verify Before Coding
- CC as a secondary diagnosis (FY2026). Can raise the stay's MS-DRG severity tier.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder structured relationships — computed from published CMS and AHRQ datasets
MS-DRG Grouper Relationships (FY2026)
Potential MS-DRG participation — not a DRG assignment.
FY2026 MS-DRG: CC — Complication or Comorbidity. Reported as a secondary diagnosis, this code raises the stay's MS-DRG severity tier — except when the principal diagnosis is one of 8 clinically related codes on its CMS exclusion list.
Named in the grouper logic of 3 MS-DRGs: DRG 698 (MDC 11), DRG 699 (MDC 11), DRG 700 (MDC 11).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):MAL003 — Genitourinary congenital anomalies (default).
Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality.
Related Codes
Same clinical process (MS-DRG)
Acts as CC — raises the severity of other admissions. CMS groups these diagnoses into one MS-DRG principal-diagnosis exclusion process — a CC/MCC on this list never raises severity when the principal diagnosis is also on it.
N13.9 — Obstructive and reflux uropathy, unspecified, Q60.0 — Renal agenesis, unilateral, Q60.1 — Renal agenesis, bilateral, Q60.2 — Renal agenesis, unspecified, Q60.3 — Renal hypoplasia, unilateral, Q60.4 — Renal hypoplasia, bilateral, Q60.6 — Potter's syndrome
Same condition, opposite side
Same category and title, differing only in which side of the body is affected.
Q60.4 — Renal hypoplasia, bilateralCompare Q60.5 vs Q60.4 →
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Genitourinary congenital anomalies).
Q56.0 — Hermaphroditism, not elsewhere classified, Q56.1 — Male pseudohermaphroditism, not elsewhere classified, Q56.2 — Female pseudohermaphroditism, not elsewhere classified, Q56.3 — Pseudohermaphroditism, unspecified, Q56.4 — Indeterminate sex, unspecified, Q60.0 — Renal agenesis, unilateral, Q60.1 — Renal agenesis, bilateral, Q60.2 — Renal agenesis, unspecified, Q60.3 — Renal hypoplasia, unilateral, Q60.4 — Renal hypoplasia, bilateral, Q60.6 — Potter's syndrome, Q61.00 — Congenital renal cyst, unspecified, Q61.01 — Congenital single renal cyst, Q61.02 — Congenital multiple renal cysts, Q61.11 — Cystic dilatation of collecting ducts, Q61.19 — Other polycystic kidney, infantile type, Q61.2 — Polycystic kidney, adult type, Q61.3 — Polycystic kidney, unspecified, Q61.4 — Renal dysplasia, Q61.5 — Medullary cystic kidney, +137 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Hypoplasia, hypoplastic”, “Atrophy, atrophic”, “Dysgenesis”; these codes share that main term but sit in a different category of the Tabular List.
Q45.8 — Other specified congenital malformations of digestive system (digestive organor tract NEC), Q50.39 — Other congenital malformation of ovary (ovary, congenital), Q51.811 — Hypoplasia of uterus (uterus, congenital), Q51.821 — Hypoplasia of cervix (cervix, congenital), Q52.4 — Other congenital malformations of vagina (vagina), Q52.79 — Other congenital malformations of vulva (vulva, congenital), Q52.8 — Other specified congenital malformations of female genitalia (genitalia, genital organ, female, congenital), Q55.1 — Hypoplasia of testis and scrotum (testis), Q55.4 — Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate (epididymis), Q55.62 — Hypoplasia of penis (penis), Q62.8 — Other congenital malformations of ureter (ureter), Q67.4 — Other congenital deformities of skull, face and jaw (hemifacial), Q73.8 — Other reduction defects of unspecified limb(s) (limb), Q74.0 — Other congenital malformations of upper limb(s), including shoulder girdle (scapula), Q74.1 — Congenital malformation of knee (patella), Q74.2 — Other congenital malformations of lower limb(s), including pelvic girdle (pelvis, pelvic girdle), Q75.8 — Other specified congenital malformations of skull and face bones (skull), Q76.49 — Other congenital malformations of spine, not associated with scoliosis (spine), Q76.6 — Other congenital malformations of ribs (rib), Q76.7 — Congenital malformation of sternum (sternum), +217 more
Contextual Map
Every relationship of Q60.5 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Hierarchy
- Q00-QA1 — Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q60-Q64 — Congenital malformations of the urinary system[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Clinical classification (CCSR)
- MAL003 — Genitourinary congenital anomalies[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- CC — Complication or Comorbidity [MS-DRG severity]: “As a secondary diagnosis this code can raise the stay's MS-DRG severity tier (CC).”— CMS MS-DRG Definitions Manual (Appendix C) · FY2026
- DRG 698 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH MCC[MS-DRG]: “OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH MCC (MDC 11)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 699 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH CC[MS-DRG]: “OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH CC (MDC 11)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 700 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITHOUT CC/MCC[MS-DRG]: “OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITHOUT CC/MCC (MDC 11)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 11 — Diseases and Disorders of the Kidney and Urinary Tract[MDC crossing]: “Diseases and Disorders of the Kidney and Urinary Tract — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 3,574 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries
- Atrophy, atrophic (of), kidney (senile) (terminal), congenital or infantile[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Dysgenesis, renal[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Hypoplasia, hypoplastic, kidney (s)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
Nearest codes
- Q60 — Renal agenesis and other reduction defects of kidney[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q60.0 — Renal agenesis, unilateral[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q60.1 — Renal agenesis, bilateral[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q60.2 — Renal agenesis, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q60.3 — Renal hypoplasia, unilateral[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q60.4 — Renal hypoplasia, bilateral[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q60.6 — Potter's syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 2026) Release, file and checksum · Publisher’s page
- Inpatient payment groups Official source data
- CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v43 Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder structured relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "Q60.5 — Renal hypoplasia, unspecified." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/q60.5-renal-hypoplasia-unspecified
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionRenal hypoplasia, unspecified
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027 (effective October 1, 2026), and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to Q60.5 in its code family, with their registry titles.