M35.7 ICD-10-CM Code: Hypermobility syndrome
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 5 inclusion terms · 3 Excludes1 · 1 Excludes2
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 557 — TENDONITIS, MYOSITIS AND BURSITIS WITH MCC (MDC 08)
- MS-DRG 558 — TENDONITIS, MYOSITIS AND BURSITIS WITHOUT MCC (MDC 08)
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 M35.7 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 M35.7 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.
- autoimmune disease NOS
- collagen (vascular) disease NOS
- systemic autoimmune disease
- systemic collagen (vascular) disease
Source: inherited from M30-M36
Inclusion Terms
Alternative terms the tabular list files under this code.
- Familial ligamentous laxity
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).
- ligamentous laxity, NOS (M24.2-) Compare M35.7 vs M24.2 →
- reactive perforating collagenosis (L87.1) inherited from M35Compare M35.7 vs L87.1 →
- autoimmune disease, single organ or single cell-type -code to relevant condition category inherited from M30-M36
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- Ehlers-Danlos syndromes (Q79.6-) Compare M35.7 vs Q79.6 →
Coder workflow for M35.7
MedCoder structured workflow — derived from this code’s own official record
Before you code M35.7
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with M35.7. 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 M35.7’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 M35.7. 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 M35.7(3 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with M35.7: 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
Excludes2 — not part of M35.7(1 note)
Coding workflow: The conditions named in this note are not included in M35.7. 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 M35.7 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 (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
- 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 M35.7 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 Excludes1 notes across 2 chapters: L94 — Other localized connective tissue disorders (via M35.-), M24.2 — Disorder of ligament.
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 2 Excludes2 notes across 2 chapters: I77 — Other disorders of arteries and arterioles (via M35.-), J82 — Pulmonary eosinophilia, not elsewhere classified (via M35.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 1 Code First instruction: J84.170 — Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere (via M35.-).
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 2 MS-DRGs: DRG 557 (MDC 08), DRG 558 (MDC 08).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):MUS024 — Systemic lupus erythematosus and connective tissue 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 clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Systemic lupus erythematosus and connective tissue disorders).
M35.05 — Sjögren syndrome with inflammatory arthritis, M35.06 — Sjögren syndrome with peripheral nervous system involvement, M35.07 — Sjögren syndrome with central nervous system involvement, M35.08 — Sjögren syndrome with gastrointestinal involvement, M35.09 — Sjögren syndrome with other organ involvement, M35.0A — Sjögren syndrome with glomerular disease, M35.0B — Sjögren syndrome with vasculitis, M35.0C — Sjögren syndrome with dental involvement, M35.1 — Other overlap syndromes, M35.2 — Behçet's disease, M35.3 — Polymyalgia rheumatica, M35.4 — Diffuse (eosinophilic) fasciitis, M35.5 — Multifocal fibrosclerosis, M35.6 — Relapsing panniculitis [Weber-Christian], M35.8 — Other specified systemic involvement of connective tissue, M35.81 — Multisystem inflammatory syndrome, M35.89 — Other specified systemic involvement of connective tissue, M35.9 — Systemic involvement of connective tissue, unspecified, M36.0 — Dermato(poly)myositis in neoplastic disease, M36.8 — Systemic disorders of connective tissue in other diseases classified elsewhere, +72 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Hypermobility, hypermotility”, “Lax, laxity”; these codes share that main term but sit in a different category of the Tabular List.
F45.8 — Other somatoform disorders (colon, psychogenic), K31.89 — Other diseases of stomach and duodenum (stomach), K58.9 — Irritable bowel syndrome, unspecified (ileum), L57.4 — Cutis laxa senilis (skin), N36.41 — Hypermobility of urethra (urethra), N36.43 — Combined hypermobility of urethra and intrinsic sphincter deficiency (urethra, with intrinsic sphincter deficiency), Q82.8 — Other specified congenital malformations of skin (skin, congenital)
Contextual Map
Every relationship of M35.7 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 M35.7 with these 6 related codes in Claim Check
Hierarchy
- M00-M99 — Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (M00-M99) (M00-M99)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- M30-M36 — Systemic connective tissue disorders[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Excludes1
- M24.2 — Disorder of ligament[Excludes1]: “ligamentous laxity, NOS (M24.2-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Excludes2
- Q79.6 — Ehlers-Danlos syndromes[Excludes2]: “Ehlers-Danlos syndromes (Q79.6-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes1 notes
- L94 — Other localized connective tissue disorders[Excludes1](via M35.-): “systemic connective tissue disorders (M30-M36)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M24.2 — Disorder of ligament[Excludes1]: “familial ligamentous laxity (M35.7)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes2 notes
- I77 — Other disorders of arteries and arterioles[Excludes2](via M35.-): “collagen (vascular) diseases (M30-M36)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- J82 — Pulmonary eosinophilia, not elsewhere classified[Excludes2](via M35.-): “pulmonary eosinophilia due to systemic connective tissue disorders (M30-M36)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Code First instructions
- J84.170 — Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere[Code First](via M35.-): “systemic connective tissue disorders (M30-M36)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Clinical classification (CCSR)
- MUS024 — Systemic lupus erythematosus and connective tissue disorders[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 557 — TENDONITIS, MYOSITIS AND BURSITIS WITH MCC[MS-DRG]: “TENDONITIS, MYOSITIS AND BURSITIS WITH MCC (MDC 08)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 558 — TENDONITIS, MYOSITIS AND BURSITIS WITHOUT MCC[MS-DRG]: “TENDONITIS, MYOSITIS AND BURSITIS WITHOUT MCC (MDC 08)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 08 — Diseases and Disorders of the Musculoskeletal System and Connective Tissue[MDC crossing]: “Diseases and Disorders of the Musculoskeletal System and Connective Tissue — 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. 18,508 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries
- Hypermobility, hypermotility, syndrome[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Lax, laxity, ligament (ous), familial[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Syndrome, hypermobility[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
Nearest codes (25)
- M35 — Other systemic involvement of connective tissue[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- M35.0 — Sjögren syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- M35.00 — Sjögren syndrome, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- M35.01 — Sjögren syndrome with keratoconjunctivitis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- M35.02 — Sjögren syndrome with lung involvement[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- M35.03 — Sjögren syndrome with myopathy[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- M35.04 — Sjögren syndrome with tubulo-interstitial nephropathy[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- M35.05 — Sjögren syndrome with inflammatory arthritis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 17 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
- 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. "M35.7 — Hypermobility syndrome." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/m35.7-hypermobility-syndrome
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionHypermobility syndrome
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 M35.7 in its code family, with their registry titles.
- M35.1 — Other overlap syndromes
- M35.2 — Behçet's disease
- M35.3 — Polymyalgia rheumatica
- M35.4 — Diffuse (eosinophilic) fasciitis
- M35.5 — Multifocal fibrosclerosis
- M35.6 — Relapsing panniculitis [Weber-Christian]
- M35.8 — Other specified systemic involvement of connective tissue
- M35.81 — Multisystem inflammatory syndrome
- M35.89 — Other specified systemic involvement of connective tissue
- M35.9 — Systemic involvement of connective tissue, unspecified