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E83.824 ICD-10-CM Code: ABCC6 deficiency causing pseudoxanthoma elasticum

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

Coding at a Glance

Tabular directives
8 Excludes1 · 1 Excludes2
Risk adjustment
CMS-HCC V22 category 23 · RxHCC V08 category 43

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 642 — INBORN AND OTHER DISORDERS OF METABOLISM (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.

Coding instructions

Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for E83.824 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 E83.824 itself; “inherited from” names the category or block whose note applies here.

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 E70-E88

Coder workflow for E83.824

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

Before you code E83.824

  1. Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E83.824. 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 E83.824’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.

    ReviewE55, E34.5, E25.0, D55, Q87.4, E29.1

Consider E83.824. 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 E83.824(8 notes)

    Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E83.824: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.

    CompareE55, E34.5, E25.0, D55, Q87.4, E29.1

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

  • Excludes2 — not part of E83.824(1 note)

    Coding workflow: The conditions named in this note are not included in E83.824. When the record documents both, both may be reported; the note is a boundary, not a prohibition.

    CompareQ79.6

    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 E83.824 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).

ReviewE55, E34.5, E25.0, D55, Q87.4, E29.1

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

ABCC6 deficiency causing pseudoxanthoma elasticum is a billable ICD-10-CM diagnosis code (E83.824).

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 (1)

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

  • 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 E83.824 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 3 Excludes1 notes across 3 chapters: E61 — Deficiency of other nutrient elements (via E83.-), P59 — Neonatal jaundice from other and unspecified causes (via E83.-), R79.0 — Abnormal level of blood mineral (via E83.-).

These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.

Referenced by 8 Excludes2 notes across 5 chapters: E83.3 — Disorders of phosphorus metabolism and phosphatases (via E83.82.-), G11 — Hereditary ataxia (via E83.-), G71 — Primary disorders of muscles (via E83.-), I70.9 — Other and unspecified atherosclerosis (via E83.82.-), N25.0 — Renal osteodystrophy (via E83.-), N25.81 — Secondary hyperparathyroidism of renal origin (via E83.-), Q28.8 — Other specified congenital malformations of circulatory system (via E83.82.-), Q82.8 — Other specified congenital malformations of skin (via E83.82.-).

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

Referenced by 2 Code First instructions across 2 chapters: G63 — Polyneuropathy in diseases classified elsewhere (via E83.-), H42 — Glaucoma in diseases classified elsewhere (via E83.-).

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 1 MS-DRG: DRG 642 (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):END016 — Other specified and unspecified nutritional and metabolic disorders (default); MUS024 — Systemic lupus erythematosus and connective tissue disorders.

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 categories (Other specified and unspecified nutritional and metabolic disorders, Systemic lupus erythematosus and connective tissue disorders).

E83.49 — Other disorders of magnesium metabolism, E83.50 — Unspecified disorder of calcium metabolism, E83.51 — Hypocalcemia, E83.52 — Hypercalcemia, E83.59 — Other disorders of calcium metabolism, E83.81 — Hungry bone syndrome, E83.820 — Generalized arterial calcification of infancy with unspecified genetic causality, E83.821 — ENPP1 deficiency causing generalized arterial calcification of infancy, E83.822 — ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2, E83.823 — ABCC6 deficiency causing generalized arterial calcification of infancy, E83.825 — CD73 deficiency causing arterial calcification, E83.89 — Other disorders of mineral metabolism, E83.9 — Disorder of mineral metabolism, unspecified, E85.0 — Non-neuropathic heredofamilial amyloidosis, E85.1 — Neuropathic heredofamilial amyloidosis, E85.2 — Heredofamilial amyloidosis, unspecified, E85.3 — Secondary systemic amyloidosis, E85.4 — Organ-limited amyloidosis, E85.8 — Other amyloidosis, E85.81 — Light chain (AL) amyloidosis, +350 more

Same Index main term, other category

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

E75.240 — Niemann-Pick disease type A (acid sphingomyelinase, type, A), E75.241 — Niemann-Pick disease type B (acid sphingomyelinase, type, B), E75.244 — Niemann-Pick disease type A/B (acid sphingomyelinase, type, A/B), E75.249 — Niemann-Pick disease, unspecified (acid sphingomyelinase), E75.26 — Sulfatase deficiency (sulfatase), E76.29 — Other mucopolysaccharidoses (beta-glucuronidase), E78.6 — Lipoprotein deficiency (lipoprotein), E79.1 — Lesch-Nyhan syndrome (hypoxanthine-), E79.2 — Myoadenylate deaminase deficiency (myoadenylate deaminase), E80.5 — Crigler-Najjar syndrome (glucuronyl transferase), E87.1 — Hypo-osmolality and hyponatremia (salt), E87.6 — Hypokalemia (kalium), E88.01 — Alpha-1-antitrypsin deficiency (alpha-1-antitrypsin), E88.02 — Plasminogen deficiency (plasminogen), E88.09 — Other disorders of plasma-protein metabolism, not elsewhere classified (pseudocholinesterase), E88.89 — Other specified metabolic disorders (dihydropyrimidine dehydrogenase), F09 — Unspecified mental disorder due to known physiological condition (cognitive), F60.2 — Antisocial personality disorder (moral), F98.8 — Other specified behavioral and emotional disorders with onset usually occurring in childhood and adolescence (attention), G96.89 — Other specified disorders of central nervous system (central nervous system), +167 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.

Gamma-glutamyl Transferase (GGT) Test

Contextual Map

Every relationship of E83.824 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 E83.824 with these 13 related codes in Claim Check

Hierarchy

Referenced by Excludes1 notes

Referenced by Excludes2 notes

Referenced by Code First instructions

Clinical classification (CCSR)

MS-DRG Grouper

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

  • Deficiency, deficient, ABCC6, pseudoxanthoma elasticum[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026

Nearest codes (39)

Change history

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. "E83.824 — ABCC6 deficiency causing pseudoxanthoma elasticum." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/e83.824-abcc6-deficiency-causing-pseudoxanthoma-elasticum

Change history

  • FY2026 — October 1, 2025
    Added to the code set
    ABCC6 deficiency causing pseudoxanthoma elasticum
    FY2026 changes

Nearest Codes in This Family

Official ICD-10-CM classifications closest to E83.824 in its code family, with their registry titles.

View all codes in the E83 family