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D72.0 ICD-10-CM Code: Genetic anomalies of leukocytes

Compare with another code for D72.0Check this code on a claim

Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.

Coding at a Glance

Tabular directives
9 inclusion terms · 4 Excludes1 · 1 Excludes2
Risk adjustment
CMS-HCC V28: 1 category · CMS-HCC V22 category 47

Billable · FY2027A valid, specific ICD-10-CM code, reportable for dates of service in FY2027.

What you need to know

Source: CMS/NCHS Official ICD-10-CM tabular notes, quoted. From the CMS/NCHS tabular list for the release in force. A note the category or block publishes applies to this code too, and is marked with where it comes from.

Excludes1Not reported with this code unless documented as unrelated
  • Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
  • basophilia (D72.824) (from D72)
  • immunity disorders (D80-D89) (from D72)
  • preleukemia (syndrome) (D46.9) (from D72)
Excludes2from D72Not included here; may be reported together
  • neutropenia (D70)
IncludesWhat this code covers
  • Alder (granulation) (granulocyte) anomaly
  • Alder syndrome
  • Hereditary leukocytic hypersegmentation
  • Hereditary leukocytic hyposegmentation

+5 more in Instructions

Where it sits Source: CMS/NCHS

Under:Chapter 3: Diseases of the Blood and Blood-forming Organs and Certain Disorders Involving the Immune MechanismD70-D77 Other disorders of blood and blood-forming organsD72 Other disorders of white blood cells

Most relevant related codes MedCoder-derived

Read off the official notes above and this code’s own position in the tabular list. Which to report is a documentation question; Compare shows the two side by side.

CompareCheck ClaimView Related Codes

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 v44, Appendix B.

  • MS-DRG 808 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH MCC (MDC 16)
  • MS-DRG 809 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH CC (MDC 16)
  • MS-DRG 810 — MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITHOUT CC/MCC (MDC 16)

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.

Risk Adjustment (CMS-HCC)

Payment categories this diagnosis maps to under CMS-HCC V28, payment year 2026.

  • HCC 115 — Specified Immunodeficiencies and White Blood Cell Disorders

Other models: CMS-HCC V22 HCC 47

Risk scores depend on the enrollee's full accepted diagnosis set and segment; a category mapping alone does not determine payment.

Coding instructions

Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for D72.0 in the official ICD-10-CM tabular list, quoted as published.

Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026

Trace:FY2027 changesChange historyRelease, file and checksum

Notes without a marker are published on D72.0 itself; “inherited from” names the category or block whose note applies here.

Inclusion Terms

Alternative terms the tabular list files under this code.

  • Alder (granulation) (granulocyte) anomaly
  • Alder syndrome
  • Hereditary leukocytic hypersegmentation
  • Hereditary leukocytic hyposegmentation
  • Hereditary leukomelanopathy
  • May-Hegglin (granulation) (granulocyte) anomaly
  • May-Hegglin syndrome
  • Pelger-Huët (granulation) (granulocyte) anomaly
  • Pelger-Huët syndrome

Excludes1 — Not Coded Here

Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).

Excludes2 — Not Included Here

Conditions not covered by this code, but which may be reported alongside it when both are present.

Source: inherited from D72

Coder workflow for D72.0

MedCoder structured workflow — derived from this code’s own official record

Before you code D72.0

  1. Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with D72.0. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).

    See the official tabular notes

Choose the right path

  1. Does the documentation support a condition named in D72.0’s Excludes1 note?
    Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
    No → Continue.

    ReviewE70.330, D72.824, D46.9

Consider D72.0. 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).

Official instructions as workflow

  • Excludes1 — check before selecting D72.0(4 notes)

    Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with D72.0: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.

    CompareE70.330, D72.824, D46.9

    See the official tabular notes · Guidelines I.A.12.a

  • Excludes2 — not part of D72.0(1 note)

    Coding workflow: The conditions named in this note are not included in D72.0. When the record documents both, both may be reported; the note is a boundary, not a prohibition.

    CompareD70

    See the official tabular notes · Guidelines I.A.12.b

Coding decision scenarios

Pattern scenarios for this code’s structure — decision rules, not clinical cases

Documentation: Both the condition D72.0 describes and a condition named in its Excludes1 note are documented for the same encounter.

Coding question: Can both codes be reported?

Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.

Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).

ReviewE70.330, D72.824, D46.9

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.

Don’t confuse D72.0 with…

MedCoder analysis — pairs from this code’s official notes, distinctions written by MedCoder

The codes most likely to be picked instead of D72.0 — named in its own official notes, or sharing its laterality or encounter family — with what separates them and which documentation moves the case. Each links to the full comparison.

  • E70.330— Excludes1 conflict (Excludes1 — generally not reported together)

    Not coded here — the tabular list excludes this pair for the same encounter.

    Not reported together with this code, except where the two conditions are documented as unrelated.

    What moves you there: Documentation of Chédiak (-Steinbrinck)-Higashi syndrome moves the case to E70.330; the two are not reported together unless documented as unrelated.

    Full comparison: D72.0 vs E70.330 →

  • D72.824— Excludes1 conflict (Excludes1 — generally not reported together)

    Not coded here — the tabular list excludes this pair for the same encounter.

    Not reported together with this code, except where the two conditions are documented as unrelated.

    What moves you there: Documentation of basophilia moves the case to D72.824; the two are not reported together unless documented as unrelated.

    Full comparison: D72.0 vs D72.824 →

  • D80— Excludes1 conflict (Excludes1 — generally not reported together)

    Not coded here — the tabular list excludes this pair for the same encounter.

    Not reported together with this code, except where the two conditions are documented as unrelated.

    What moves you there: Documentation of immunity disorders moves the case to D80; the two are not reported together unless documented as unrelated.

    Full comparison: D72.0 vs D80 →

  • D89— Excludes1 conflict (Excludes1 — generally not reported together)

    Not coded here — the tabular list excludes this pair for the same encounter.

    Not reported together with this code, except where the two conditions are documented as unrelated.

    What moves you there: Documentation of immunity disorders moves the case to D89; the two are not reported together unless documented as unrelated.

    Full comparison: D72.0 vs D89 →

  • D46.9— Excludes1 conflict (Excludes1 — generally not reported together)

    Not coded here — the tabular list excludes this pair for the same encounter.

    Not reported together with this code, except where the two conditions are documented as unrelated.

    What moves you there: Documentation of preleukemia (syndrome) moves the case to D46.9; the two are not reported together unless documented as unrelated.

    Full comparison: D72.0 vs D46.9 →

  • D72.9— Specificity relationship (Review)

    Overlapping diagnoses in the same category.

    Overlapping codes in the same category — the documentation decides which is the more specific fit.

    What moves you there: A record that documents no more than “Disorder of white blood cells, unspecified” takes D72.9; specificity in the record moves it back here.

    Full comparison: D72.0 vs D72.9 →

Relationships are read from this code's own official notes, its laterality siblings and its encounter family; the wording of each distinction is MedCoder editorial, and the documentation named in each “what moves you there” line is the official note phrase or sibling title itself. Source: CMS ICD-10-CM tabular instructional notes; ICD-10-CM Official Guidelines, Section I.A.12.a.

Coding context

Guidelines, coding notes, decision aids, relationships (with MS-DRG and CCSR classification), hierarchy, HCC, coverage and the context map: what a coder reaches for after the core. Each section names whether it is official source data, a MedCoder-derived relationship or MedCoder editorial.

Code Overview

Genetic anomalies of leukocytes is a billable ICD-10-CM diagnosis code (D72.0).

MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.

Official Coding Guidelines

No excerpt in the ICD-10-CM Official Guidelines names this code specifically. Its chapter carries only this chapter-wide note:

Chapter 3: Disease of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)

Reserved for future guideline expansion

Verify Before Coding

  • No Medicare Code Editor or MS-DRG Definitions Manual restrictions apply to this code.

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-derived relationships — computed from published CMS and AHRQ datasets

Other codes that name D72.0 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.

Referenced by 10 Excludes2 notes: R70 — Elevated erythrocyte sedimentation rate and abnormality of plasma viscosity (via D72.-), R70-R79 — Abnormal findings on examination of blood, without diagnosis (R70-R79) (via D72.-), R71 — Abnormality of red blood cells (via D72.-), R73 — Elevated blood glucose level (via D72.-), R74 — Abnormal serum enzyme levels (via D72.-), R75 — Inconclusive laboratory evidence of human immunodeficiency virus [HIV] (via D72.-), R76 — Other abnormal immunological findings in serum (via D72.-), R77 — Other abnormalities of plasma proteins (via D72.-), R78 — Findings of drugs and other substances, not normally found in blood (via D72.-), R79 — Other abnormal findings of blood chemistry (via D72.-).

These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.

Referenced by 21 Code First instructions: T36 — Poisoning by, adverse effect of and underdosing of systemic antibiotics (via D72.-), T36-T39 — Antibiotics & Anti-infectives (T36-T39) (via D72.-), T36-T50 — Poisoning by, adverse effects of and underdosing of drugs, medicaments and biological substances (T36-T50) (via D72.-), T37 — Poisoning by, adverse effect of and underdosing of other systemic anti-infectives and antiparasitics (via D72.-), T38 — Poisoning by, adverse effect of and underdosing of hormones and their synthetic substitutes and antagonists, not elsewhere classified (via D72.-), T39 — Poisoning by, adverse effect of and underdosing of nonopioid analgesics, antipyretics and antirheumatics (via D72.-), T40 — Poisoning by, adverse effect of and underdosing of narcotics and psychodysleptics [hallucinogens] (via D72.-), T40-T41 — Analgesics & Antipyretics (T40-T41) (via D72.-), T41 — Poisoning by, adverse effect of and underdosing of anesthetics and therapeutic gases (via D72.-), T42 — Poisoning by, adverse effect of and underdosing of antiepileptic, sedative- hypnotic and antiparkinsonism drugs (via D72.-), T42-T43 — Anticonvulsants & Psychotropics (T42-T43) (via D72.-), T43 — Poisoning by, adverse effect of and underdosing of psychotropic drugs, not elsewhere classified (via D72.-), T44 — Poisoning by, adverse effect of and underdosing of drugs primarily affecting the autonomic nervous system (via D72.-), T44-T46 — Cardiovascular & Gastrointestinal (T44-T46) (via D72.-), T45 — Poisoning by, adverse effect of and underdosing of primarily systemic and hematological agents, not elsewhere classified (via D72.-), T46 — Poisoning by, adverse effect of and underdosing of agents primarily affecting the cardiovascular system (via D72.-), T47 — Poisoning by, adverse effect of and underdosing of agents primarily affecting the gastrointestinal system (via D72.-), T47-T50 — Hormones & Systemic Agents (T47-T50) (via D72.-), T48 — Poisoning by, adverse effect of and underdosing of agents primarily acting on smooth and skeletal muscles and the respiratory system (via D72.-), T49 — Poisoning by, adverse effect of and underdosing of topical agents primarily affecting skin and mucous membrane and by ophthalmological, otorhinorlaryngological and dental drugs (via D72.-), +1 more.

Each of these codes carries a Code First note naming this condition — when that code is reported, THIS code is sequenced first, ahead of it.

MS-DRG Grouper Relationships (FY2027)

Potential MS-DRG participation — not a DRG assignment.

FY2027 MS-DRG: not on the CMS CC/MCC list — as a secondary diagnosis this code does not change MS-DRG severity for that release.

Named in the grouper logic of 3 MS-DRGs: DRG 808 (MDC 16), DRG 809 (MDC 16), DRG 810 (MDC 16).

From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.

Clinical classification (AHRQ CCSR):BLD007 — Diseases of white blood cells (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 CMS-HCC risk category (V28)

CMS maps these diagnoses to the same Hierarchical Condition Category (Specified Immunodeficiencies and White Blood Cell Disorders) for risk-adjusted payment.

D70.0 — Congenital agranulocytosis, D70.4 — Cyclic neutropenia, D71 — Functional disorders of polymorphonuclear neutrophils, D71.1 — Leukocyte adhesion deficiency, D71.8 — Other functional disorders of polymorphonuclear neutrophils, D71.9 — Functional disorders of polymorphonuclear neutrophils, unspecified, D76.1 — Hemophagocytic lymphohistiocytosis, D76.3 — Other histiocytosis syndromes, D80.0 — Hereditary hypogammaglobulinemia, D80.2 — Selective deficiency of immunoglobulin A [IgA], D80.3 — Selective deficiency of immunoglobulin G [IgG] subclasses, D80.4 — Selective deficiency of immunoglobulin M [IgM], D80.5 — Immunodeficiency with increased immunoglobulin M [IgM], D81.4 — Nezelof's syndrome, D82.0 — Wiskott-Aldrich syndrome, D82.1 — Di George's syndrome, D84.1 — Defects in the complement system, D89.84 — IgG4-related disease

Related risk categories

These categories interact through CMS's HCC hierarchy — one can suppress the other's risk-adjustment weight when both are present on a claim.

Common Variable and Combined Immunodeficiencies

Same clinical category (CCSR)

AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Diseases of white blood cells).

D70.1 — Agranulocytosis secondary to cancer chemotherapy, D70.2 — Other drug-induced agranulocytosis, D70.3 — Neutropenia due to infection, D70.4 — Cyclic neutropenia, D70.8 — Other neutropenia, D70.9 — Neutropenia, unspecified, D71 — Functional disorders of polymorphonuclear neutrophils, D71.1 — Leukocyte adhesion deficiency, D71.8 — Other functional disorders of polymorphonuclear neutrophils, D71.9 — Functional disorders of polymorphonuclear neutrophils, unspecified, D72.1 — Eosinophilia, D72.10 — Eosinophilia, unspecified, D72.110 — Idiopathic hypereosinophilic syndrome [IHES], D72.111 — Lymphocytic Variant Hypereosinophilic Syndrome [LHES], D72.118 — Other hypereosinophilic syndrome, D72.119 — Hypereosinophilic syndrome [HES], unspecified, D72.12 — Drug rash with eosinophilia and systemic symptoms syndrome, D72.18 — Eosinophilia in diseases classified elsewhere, D72.19 — Other eosinophilia, D72.810 — Lymphocytopenia, +17 more

Same Index main term, other category

The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Anomaly, anomalous”, “Dysgenesis”; these codes share that main term but sit in a different category of the Tabular List.

A50.56 — Late congenital syphilitic osteochondropathy (tibia NEC, saber), A50.57 — Syphilitic saddle nose (saddle nose, syphilitic), D69.3 — Immune thrombocytopenic purpura (tidal platelet), E64.3 — Sequelae of rickets (pelvis NEC, rachitic), E70.330 — Chediak-Higashi syndrome (Chédiak-Higashi), H57.00 — Unspecified anomaly of pupillary function (pupil, function), H57.01 — Argyll Robertson pupil, atypical (pupil, function, Argyll Robertson pupil), H57.02 — Anisocoria (pupil, function, anisocoria), H57.03 — Miosis (pupil, function, miosis), H57.04 — Mydriasis (pupil, function, mydriasis), H57.05 — Tonic pupil (pupil, function, tonic pupil), H57.09 — Other anomalies of pupillary function (pupil, function, specified type NEC), I42.4 — Endocardial fibroelastosis (heart, fibroelastosis cordis), I45.6 — Pre-excitation syndrome (atrioventricular, excitation), K00.2 — Abnormalities of size and form of teeth (form, teeth), K00.6 — Disturbances in tooth eruption (tooth, teeth, eruption), K00.9 — Disorder of tooth development, unspecified (tooth, teeth), K04.3 — Abnormal hard tissue formation in pulp (hard tissue formation in pulp), L81.9 — Disorder of pigmentation, unspecified (pigmentation), M26.00 — Unspecified anomaly of jaw size (dentofacial, jaw size), +241 more

Contextual Map

Every relationship of D72.0 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.

Run D72.0 with these 17 related codes in Claim Check

Hierarchy

Excludes1

Referenced by Excludes2 notes (10)

Referenced by Code First instructions (21)

Clinical classification (CCSR)

Risk adjustment (CMS-HCC)

  • HCC 115 — Specified Immunodeficiencies and White Blood Cell Disorders [CMS-HCC]— CMS-HCC V28 · 2026

MS-DRG Grouper

MDC crossing

  • MDC 16 — Diseases and Disorders of Blood, Blood Forming Organs and Immunologic Disorders[MDC crossing]: “Diseases and Disorders of Blood, Blood Forming Organs and Immunologic Disorders — 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. 1,615 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027

Index entries (26)

  • Alder (-Reilly) anomaly or syndrome (leukocyte granulation)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Anomaly, anomalous (congenital) (unspecified type), Alder (-Reilly) (leukocyte granulation)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Anomaly, anomalous (congenital) (unspecified type), granulation or granulocyte, genetic (constitutional) (leukocyte)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Anomaly, anomalous (congenital) (unspecified type), Hegglin's[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Anomaly, anomalous (congenital) (unspecified type), hypersegmentation of neutrophils, hereditary[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Anomaly, anomalous (congenital) (unspecified type), Jordan's[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Anomaly, anomalous (congenital) (unspecified type), leukocytes, genetic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Anomaly, anomalous (congenital) (unspecified type), leukocytes, genetic, granulation (constitutional)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • and 18 more

Nearest codes (27)

Change history

  • FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016

Reference

Index terms and tables, published questions and FAQ, every source behind this page with its release and checksum, the date-of-service check and the complete change history.

Indexed Clinical Terms (26)

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.

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 FY2027 tabular list, index and tables, effective October 1, 2026 Release, file and checksum · Publisher’s page
Coding guidelines Official source data
ICD-10-CM Official Guidelines for Coding and Reporting (FY2027), quoted by section Release, file and checksum · Publisher’s page
Claim edits Official source data
CMS Definitions of Medicare Code Edits — v44.0 (October 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 — v44 Release, file and checksum · Publisher’s page
Risk adjustment Official source data
2026 Mid-Year Final ICD-10 Mappings + Model Software (cms.gov/files/zip/2026-midyear-final-icd-10-mappings.zip, 2026-midyear-final-model-software.zip) — CMS-HCC V28, PY2026 mid-year final release 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-derived 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 editorial 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.

Current data releases:ICD-10-CM FY2027 · ICD-10-PCS FY2027 · HCPCS October 2026 · MS-DRG v44 · Medicare Code Editor v44.0 · NCCI PTP Q4 2026 · MUE Q4 2026 · NCD code lists 2026-01 · LCD export September 28, 2026 · All releases and sources

Labels on this page: Official source data · MedCoder-derived relationship · MedCoder editorial explanation. How to read the labels · All data sources and release dates · CMS coding rules

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. "D72.0 — Genetic anomalies of leukocytes." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/d72.0-genetic-anomalies-of-leukocytes

Change history

  • FY2016 — October 1, 2015
    In the code set at ICD-10-CM adoption
    Genetic anomalies of leukocytes

No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027, 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 D72.0 in its code family, with their registry titles.

View all codes in the D72 family