E31.0 ICD-10-CM Code: Autoimmune polyglandular failure
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 1 inclusion term · 5 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 643 — ENDOCRINE DISORDERS WITH MCC (MDC 10)
- MS-DRG 644 — ENDOCRINE DISORDERS WITH CC (MDC 10)
- MS-DRG 645 — ENDOCRINE DISORDERS WITHOUT CC/MCC (MDC 10)
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 51 — Addison's and Cushing's Diseases, Acromegaly, and Other Specified Endocrine Disorders
Other models: CMS-HCC V22 HCC 23 · RxHCC V08 HCC 43
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 E31.0 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 E31.0 itself; “inherited from” names the category or block whose note applies here.
Inclusion Terms
Alternative terms the tabular list files under this code.
- Schmidt's 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).
- ataxia telangiectasia Louis-Bar
- dystrophia myotonica Steinert
- pseudohypoparathyroidism (E20.1) inherited from E31Compare E31.0 vs E20.1 →
- galactorrhea (N64.3) inherited from E20-E35Compare E31.0 vs N64.3 →
- gynecomastia (N62) inherited from E20-E35Compare E31.0 vs N62 →
Coder workflow for E31.0
MedCoder structured workflow — derived from this code’s own official record
Before you code E31.0
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E31.0. 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 documentation support a condition named in E31.0’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.
Consider E31.0. 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 E31.0(5 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E31.0: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
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: Both the condition E31.0 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).
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 (10)
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.
- Atrophy, atrophic (of), pluriglandular, autoimmune
- Deficiency, deficient, polyglandular, autoimmune
- Failure, failed, polyglandular, autoimmune
- Insufficiency, insufficient, progressive pluriglandular
- Polyglandular, deficiency
- Schmidt's syndrome (polyglandular, autoimmune)
- Syndrome, autoimmune polyglandular
- Syndrome, pluriglandular (compensatory), autoimmune
- Syndrome, polyglandular, autoimmune
- Syndrome, thyroid-adrenocortical insufficiency
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 E31.0 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 2 Code First instructions across 2 chapters: E20.812 — Autoimmune hypoparathyroidism, G63 — Polyneuropathy in diseases classified elsewhere (via E31.-).
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 3 MS-DRGs: DRG 643 (MDC 10), DRG 644 (MDC 10), DRG 645 (MDC 10).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):END015 — Other specified and unspecified endocrine disorders (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 (Addison's and Cushing's Diseases, Acromegaly, and Other Specified Endocrine Disorders) for risk-adjusted payment.
E22.0 — Acromegaly and pituitary gigantism, E24.0 — Pituitary-dependent Cushing's disease, E27.1 — Primary adrenocortical insufficiency, E31.1 — Polyglandular hyperfunction, E31.20 — Multiple endocrine neoplasia [MEN] syndrome, unspecified, E31.21 — Multiple endocrine neoplasia [MEN] type I, E31.22 — Multiple endocrine neoplasia [MEN] type IIA, E31.23 — Multiple endocrine neoplasia [MEN] type IIB, E31.8 — Other polyglandular dysfunction, E31.9 — Polyglandular dysfunction, unspecified
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Other specified and unspecified endocrine disorders).
E28.8 — Other ovarian dysfunction, E28.9 — Ovarian dysfunction, unspecified, E29.0 — Testicular hyperfunction, E29.1 — Testicular hypofunction, E29.8 — Other testicular dysfunction, E29.9 — Testicular dysfunction, unspecified, E30.0 — Delayed puberty, E30.1 — Precocious puberty, E30.8 — Other disorders of puberty, E30.9 — Disorder of puberty, unspecified, E31.1 — Polyglandular hyperfunction, E31.20 — Multiple endocrine neoplasia [MEN] syndrome, unspecified, E31.21 — Multiple endocrine neoplasia [MEN] type I, E31.22 — Multiple endocrine neoplasia [MEN] type IIA, E31.23 — Multiple endocrine neoplasia [MEN] type IIB, E31.8 — Other polyglandular dysfunction, E31.9 — Polyglandular dysfunction, unspecified, E32.0 — Persistent hyperplasia of thymus, E32.1 — Abscess of thymus, E32.8 — Other diseases of thymus, +83 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Failure, failed”, “Atrophy, atrophic”, “Deficiency, deficient”, …; these codes share that main term but sit in a different category of the Tabular List.
E20.9 — Hypoparathyroidism, unspecified (parathyroid), E23.0 — Hypopituitarism (gonadotropin), E23.2 — Diabetes insipidus (vasopressin), E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency (11-hydroxylase), E27.1 — Primary adrenocortical insufficiency (adrenal, primary), E27.3 — Drug-induced adrenocortical insufficiency (adrenocortical, iatrogenic), E27.40 — Unspecified adrenocortical insufficiency (adrenal), E27.49 — Other adrenocortical insufficiency (adrenal), E28.39 — Other primary ovarian failure (ovarian), E29.1 — Testicular hypofunction (testis), E32.0 — Persistent hyperplasia of thymus (involution, thymus), E32.8 — Other diseases of thymus (thymus), E34.328 — Other genetic causes of short stature (short stature homeobox gene, with, short stature), E34.9 — Endocrine disorder, unspecified (endocrine), E41 — Nutritional marasmus (infantile), E42 — Marasmic kwashiorkor (calorie, severe, with marasmus, and kwashiorkor), E43 — Unspecified severe protein-calorie malnutrition (nutritional), E46 — Unspecified protein-calorie malnutrition (protein), E50.0 — Vitamin A deficiency with conjunctival xerosis (vitamin NOS, A, with, xerosis, conjunctival), E50.1 — Vitamin A deficiency with Bitot's spot and conjunctival xerosis (vitamin NOS, A, with, Bitot's spot), +525 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.
HbA1c Test (Glycated Hemoglobin), Thyroid Stimulating Hormone (TSH)
Contextual Map
Every relationship of E31.0 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 E31.0 with these 2 related codes in Claim Check
Hierarchy
- E00-E89 — Chapter 4: Endocrine, Nutritional and Metabolic Diseases (E00-E89) (E00-E89)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E20-E35 — Disorders of other endocrine glands[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Referenced by Code First instructions
- E20.812 — Autoimmune hypoparathyroidism[Code First]: “autoimmune polyglandular failure (E31.0)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- G63 — Polyneuropathy in diseases classified elsewhere[Code First](via E31.-): “endocrine disease, except diabetes (E00-E07, E15-E16, E20-E34)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Clinical classification (CCSR)
- END015 — Other specified and unspecified endocrine disorders[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
Risk adjustment (CMS-HCC)
- HCC 51 — Addison's and Cushing's Diseases, Acromegaly, and Other Specified Endocrine Disorders [CMS-HCC]— CMS-HCC V28 · 2026
MS-DRG Grouper
- DRG 643 — ENDOCRINE DISORDERS WITH MCC[MS-DRG]: “ENDOCRINE DISORDERS WITH MCC (MDC 10)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 644 — ENDOCRINE DISORDERS WITH CC[MS-DRG]: “ENDOCRINE DISORDERS WITH CC (MDC 10)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 645 — ENDOCRINE DISORDERS WITHOUT CC/MCC[MS-DRG]: “ENDOCRINE DISORDERS WITHOUT CC/MCC (MDC 10)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 10 — Endocrine, Nutritional and Metabolic Diseases and Disorders[MDC crossing]: “Endocrine, Nutritional and Metabolic Diseases and 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. 5,008 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries (10)
- Atrophy, atrophic (of), pluriglandular, autoimmune[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Deficiency, deficient, polyglandular, autoimmune[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Failure, failed, polyglandular, autoimmune[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Insufficiency, insufficient, progressive pluriglandular[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Polyglandular, deficiency[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Schmidt's syndrome (polyglandular, autoimmune)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Syndrome, autoimmune polyglandular[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Syndrome, pluriglandular (compensatory), autoimmune[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- and 2 more
Nearest codes (9)
- E31 — Polyglandular dysfunction[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E31.1 — Polyglandular hyperfunction[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E31.2 — Multiple endocrine neoplasia [MEN] syndromes[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E31.20 — Multiple endocrine neoplasia [MEN] syndrome, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E31.21 — Multiple endocrine neoplasia [MEN] type I[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E31.22 — Multiple endocrine neoplasia [MEN] type IIA[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E31.23 — Multiple endocrine neoplasia [MEN] type IIB[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E31.8 — Other polyglandular dysfunction[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 1 more
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
- 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 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. "E31.0 — Autoimmune polyglandular failure." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/e31.0-autoimmune-polyglandular-failure
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionAutoimmune polyglandular failure
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 E31.0 in its code family, with their registry titles.
- E31 — Polyglandular dysfunction
- E31.1 — Polyglandular hyperfunction
- E31.2 — Multiple endocrine neoplasia [MEN] syndromes
- E31.20 — Multiple endocrine neoplasia [MEN] syndrome, unspecified
- E31.21 — Multiple endocrine neoplasia [MEN] type I
- E31.22 — Multiple endocrine neoplasia [MEN] type IIA
- E31.23 — Multiple endocrine neoplasia [MEN] type IIB
- E31.8 — Other polyglandular dysfunction
- E31.9 — Polyglandular dysfunction, unspecified