D56.9 ICD-10-CM Code: Thalassemia, unspecified
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 1 inclusion term · 1 Excludes1
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 791 — PREMATURITY WITH MAJOR PROBLEMS (MDC 15)
- MS-DRG 793 — FULL TERM NEONATE WITH MAJOR PROBLEMS (MDC 15)
- MS-DRG 811 — RED BLOOD CELL DISORDERS WITH MCC (MDC 16)
- MS-DRG 812 — RED BLOOD CELL DISORDERS WITHOUT 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.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for D56.9 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 D56.9 itself; “inherited from” names the category or block whose note applies here.
Inclusion Terms
Alternative terms the tabular list files under this code.
- Mediterranean anemia (with other hemoglobinopathy)
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).
- sickle-cell thalassemia (D57.4-) Compare D56.9 vs D57.4 →
Source: inherited from D56
Coder workflow for D56.9
MedCoder structured workflow — derived from this code’s own official record
Before you code D56.9
- Unspecified does not mean incorrect. When the record gives no greater specificity, D56.9 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).
ReviewD56.0, D56.1, D56.2, D56.3, D56.4, D56.5, D56.8
See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with D56.9. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
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 — D56.9 is appropriate when the documentation goes no further. - Does the documentation support a condition named in D56.9’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.ReviewD57.4
Consider D56.9. 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).
- 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.
Official instructions as workflow
Excludes1 — check before selecting D56.9(1 note)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with D56.9: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareD57.4
See the official tabular notes · Guidelines I.A.12.a
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: Both the condition D56.9 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).
ReviewD57.4
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 (12)
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.
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), Mediterranean (with other hemoglobinopathy)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), microelliptopoikilocytic (Rietti-Greppi- Micheli)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), Rietti-Greppi-Micheli
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), thalassemia
- Arthritis, arthritic (acute) (chronic) (nonpyogenic) (subacute), in (due to), thalassemia NEC
- Disease, diseased, hemoglobin or Hb, abnormal NEC (mixed), with thalassemia
- Disease, diseased, hemoglobin or Hb, H (Hb-H) (thalassemia), with other abnormal hemoglobin NEC
- Disease, diseased, hemoglobin or Hb, I thalassemia
- Disease, diseased, high fetal gene or hemoglobin thalassemia
- Leptocytosis, hereditary
- Rietti-Greppi-Micheli anemia
- Thalassemia (anemia) (disease)
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 structured relationships — computed from published CMS and AHRQ datasets
Other codes that name D56.9 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 14 Excludes1 notes across 2 chapters: P50 — Newborn affected by intrauterine (fetal) blood loss (via D56.-), P50-P61 — Hemorrhagic and hematological disorders of newborn (P50-P61) (via D56.-), P51 — Umbilical hemorrhage of newborn (via D56.-), P52 — Intracranial nontraumatic hemorrhage of newborn (via D56.-), P53 — Hemorrhagic disease of newborn (via D56.-), P54 — Other neonatal hemorrhages (via D56.-), P55 — Hemolytic disease of newborn (via D56.-), P56 — Hydrops fetalis due to hemolytic disease (via D56.-), P57 — Kernicterus (via D56.-), P58 — Neonatal jaundice due to other excessive hemolysis (via D56.-), P59 — Neonatal jaundice from other and unspecified causes (via D56.-), P60 — Disseminated intravascular coagulation of newborn (via D56.-), P61 — Other perinatal hematological disorders (via D56.-), R71 — Abnormality of red blood cells (via D56.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 24 Code First instructions across 3 chapters: I21.A1 — Myocardial infarction type 2 (via D56.-), M36.3 — Arthropathy in other blood disorders (via D56.-), M90.5 — Osteonecrosis in diseases classified elsewhere (via D56.-), T36 — Poisoning by, adverse effect of and underdosing of systemic antibiotics (via D56.-), T36-T39 — Antibiotics & Anti-infectives (T36-T39) (via D56.-), T36-T50 — Poisoning by, adverse effects of and underdosing of drugs, medicaments and biological substances (T36-T50) (via D56.-), T37 — Poisoning by, adverse effect of and underdosing of other systemic anti-infectives and antiparasitics (via D56.-), T38 — Poisoning by, adverse effect of and underdosing of hormones and their synthetic substitutes and antagonists, not elsewhere classified (via D56.-), T39 — Poisoning by, adverse effect of and underdosing of nonopioid analgesics, antipyretics and antirheumatics (via D56.-), T40 — Poisoning by, adverse effect of and underdosing of narcotics and psychodysleptics [hallucinogens] (via D56.-), T40-T41 — Analgesics & Antipyretics (T40-T41) (via D56.-), T41 — Poisoning by, adverse effect of and underdosing of anesthetics and therapeutic gases (via D56.-), T42 — Poisoning by, adverse effect of and underdosing of antiepileptic, sedative- hypnotic and antiparkinsonism drugs (via D56.-), T42-T43 — Anticonvulsants & Psychotropics (T42-T43) (via D56.-), T43 — Poisoning by, adverse effect of and underdosing of psychotropic drugs, not elsewhere classified (via D56.-), T44 — Poisoning by, adverse effect of and underdosing of drugs primarily affecting the autonomic nervous system (via D56.-), T44-T46 — Cardiovascular & Gastrointestinal (T44-T46) (via D56.-), T45 — Poisoning by, adverse effect of and underdosing of primarily systemic and hematological agents, not elsewhere classified (via D56.-), T46 — Poisoning by, adverse effect of and underdosing of agents primarily affecting the cardiovascular system (via D56.-), T47 — Poisoning by, adverse effect of and underdosing of agents primarily affecting the gastrointestinal system (via D56.-), +4 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 (FY2026)
Potential MS-DRG participation — not a DRG assignment.
FY2026 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 4 MS-DRGs: DRG 791 (MDC 15), DRG 793 (MDC 15), DRG 811 (MDC 16), DRG 812 (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):BLD002 — Hemolytic anemia (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 category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Hemolytic anemia).
D55.3 — Anemia due to disorders of nucleotide metabolism, D55.8 — Other anemias due to enzyme disorders, D55.9 — Anemia due to enzyme disorder, unspecified, D56.0 — Alpha thalassemia, D56.1 — Beta thalassemia, D56.2 — Delta-beta thalassemia, D56.3 — Thalassemia minor, D56.4 — Hereditary persistence of fetal hemoglobin [HPFH], D56.5 — Hemoglobin E-beta thalassemia, D56.8 — Other thalassemias, D58.0 — Hereditary spherocytosis, D58.1 — Hereditary elliptocytosis, D58.2 — Other hemoglobinopathies, D58.8 — Other specified hereditary hemolytic anemias, D58.9 — Hereditary hemolytic anemia, unspecified, D59.0 — Drug-induced autoimmune hemolytic anemia, D59.1 — Other autoimmune hemolytic anemias, D59.10 — Autoimmune hemolytic anemia, unspecified, D59.11 — Warm autoimmune hemolytic anemia, D59.12 — Cold autoimmune hemolytic anemia, +18 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main term “Anemia”; these codes share that main term but sit in a different category of the Tabular List.
D53.2 — Scorbutic anemia (scorbutic), D53.8 — Other specified nutritional anemias (due to, deficiency, zinc), D53.9 — Nutritional anemia, unspecified (macrocytic), D55.0 — Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency (favism), D55.1 — Anemia due to other disorders of glutathione metabolism (deficiency, G SH), D55.21 — Anemia due to pyruvate kinase deficiency (deficiency, PK), D55.29 — Anemia due to other disorders of glycolytic enzymes (deficiency, 2, 3 PG), D55.3 — Anemia due to disorders of nucleotide metabolism (deficiency, enzyme, nucleotide metabolism), D55.8 — Other anemias due to enzyme disorders (deficiency, enzyme, specified type NEC), D55.9 — Anemia due to enzyme disorder, unspecified (deficiency, enzyme), D57.1 — Sickle-cell disease without crisis (Herrick's), D57.40 — Sickle-cell thalassemia without crisis (microdrepanocytosis), D58.0 — Hereditary spherocytosis (congenital, spherocytic), D58.2 — Other hemoglobinopathies (congenital, Heinz body), D58.8 — Other specified hereditary hemolytic anemias (stomatocytosis), D58.9 — Hereditary hemolytic anemia, unspecified (childhood), D59.0 — Drug-induced autoimmune hemolytic anemia (hemolytic, autoimmune, drug-induced), D59.10 — Autoimmune hemolytic anemia, unspecified (hemolytic, autoimmune), D59.11 — Warm autoimmune hemolytic anemia (hemolytic, warm type), D59.12 — Cold autoimmune hemolytic anemia (hemolytic, cold type), +284 more
Lab tests where this diagnosis supports Medicare coverage (NCD)
Medicare's National Coverage Determination (NCD) program lists this diagnosis as medical justification for these lab tests.
Contextual Map
Every relationship of D56.9 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 D56.9 with these 16 related codes in Claim Check
Hierarchy
- D50-D89 — Chapter 3: Diseases of the Blood and Blood-forming Organs and Certain Disorders Involving the Immune Mechanism (D50-D89) (D50-D89)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D55-D59 — Hemolytic anemias[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Referenced by Excludes1 notes (14)
- P50 — Newborn affected by intrauterine (fetal) blood loss[Excludes1](via D56.-): “hereditary hemolytic anemias (D55-D58)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P50-P61 — Hemorrhagic and hematological disorders of newborn (P50-P61)[Excludes1](via D56.-): “hereditary hemolytic anemias (D55-D58)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P51 — Umbilical hemorrhage of newborn[Excludes1](via D56.-): “hereditary hemolytic anemias (D55-D58)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P52 — Intracranial nontraumatic hemorrhage of newborn[Excludes1](via D56.-): “hereditary hemolytic anemias (D55-D58)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P53 — Hemorrhagic disease of newborn[Excludes1](via D56.-): “hereditary hemolytic anemias (D55-D58)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P54 — Other neonatal hemorrhages[Excludes1](via D56.-): “hereditary hemolytic anemias (D55-D58)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P55 — Hemolytic disease of newborn[Excludes1](via D56.-): “hereditary hemolytic anemias (D55-D58)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P56 — Hydrops fetalis due to hemolytic disease[Excludes1](via D56.-): “hereditary hemolytic anemias (D55-D58)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- and 6 more
Referenced by Code First instructions (24)
- I21.A1 — Myocardial infarction type 2[Code First](via D56.-): “anemia (D50.0-D64.9)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M36.3 — Arthropathy in other blood disorders[Code First](via D56.-): “thalassemia (D56.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M90.5 — Osteonecrosis in diseases classified elsewhere[Code First](via D56.-): “hemoglobinopathy (D50-D64)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- T36 — Poisoning by, adverse effect of and underdosing of systemic antibiotics[Code First](via D56.-): “blood disorders (D56-D76)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- T36-T39 — Antibiotics & Anti-infectives (T36-T39)[Code First](via D56.-): “blood disorders (D56-D76)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- T36-T50 — Poisoning by, adverse effects of and underdosing of drugs, medicaments and biological substances (T36-T50)[Code First](via D56.-): “blood disorders (D56-D76)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- T37 — Poisoning by, adverse effect of and underdosing of other systemic anti-infectives and antiparasitics[Code First](via D56.-): “blood disorders (D56-D76)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- T38 — Poisoning by, adverse effect of and underdosing of hormones and their synthetic substitutes and antagonists, not elsewhere classified[Code First](via D56.-): “blood disorders (D56-D76)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- and 16 more
Clinical classification (CCSR)
- BLD002 — Hemolytic anemia[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 791 — PREMATURITY WITH MAJOR PROBLEMS[MS-DRG]: “PREMATURITY WITH MAJOR PROBLEMS (MDC 15)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 793 — FULL TERM NEONATE WITH MAJOR PROBLEMS[MS-DRG]: “FULL TERM NEONATE WITH MAJOR PROBLEMS (MDC 15)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 811 — RED BLOOD CELL DISORDERS WITH MCC[MS-DRG]: “RED BLOOD CELL DISORDERS WITH MCC (MDC 16)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 812 — RED BLOOD CELL DISORDERS WITHOUT MCC[MS-DRG]: “RED BLOOD CELL DISORDERS WITHOUT MCC (MDC 16)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 15 — Newborns and Other Neonates with Conditions Originating in Perinatal Period[MDC crossing]: “Newborns and Other Neonates with Conditions Originating in Perinatal Period — 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.”— CMS MS-DRG Definitions Manual · FY2026
- 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. 1,614 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries (12)
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), Mediterranean (with other hemoglobinopathy)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), microelliptopoikilocytic (Rietti-Greppi- Micheli)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), Rietti-Greppi-Micheli[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound), thalassemia[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Arthritis, arthritic (acute) (chronic) (nonpyogenic) (subacute), in (due to), thalassemia NEC[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Disease, diseased, hemoglobin or Hb, abnormal NEC (mixed), with thalassemia[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Disease, diseased, hemoglobin or Hb, H (Hb-H) (thalassemia), with other abnormal hemoglobin NEC[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Disease, diseased, hemoglobin or Hb, I thalassemia[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- and 4 more
Nearest codes
- D56 — Thalassemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D56.0 — Alpha thalassemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D56.1 — Beta thalassemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D56.2 — Delta-beta thalassemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D56.3 — Thalassemia minor[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D56.4 — Hereditary persistence of fetal hemoglobin [HPFH][Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D56.5 — Hemoglobin E-beta thalassemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- D56.8 — Other thalassemias[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
- Coding guidelines Official source data
- ICD-10-CM Official Guidelines for Coding and Reporting (FY2026), quoted by section 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. "D56.9 — Thalassemia, unspecified." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/d56.9-thalassemia-unspecified
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionThalassemia, 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 D56.9 in its code family, with their registry titles.