E34.39 ICD-10-CM Code: Other short stature due to endocrine disorder
Compare with another code for E34.39Check 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
- 14 Excludes1
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.
Where it sits Source: CMS/NCHS
Under:Chapter 4: Endocrine, Nutritional and Metabolic DiseasesE20-E35 Disorders of other endocrine glandsE34 Other endocrine disordersE34.3 Short stature due to endocrine disorder
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.
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 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.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for E34.39 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 E34.39 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).
- achondroplastic short stature (Q77.4) inherited from E34.3Compare E34.39 vs Q77.4 →
- hypochondroplastic short stature (Q77.4) inherited from E34.3Compare E34.39 vs Q77.4 →
- nutritional short stature (E45) inherited from E34.3Compare E34.39 vs E45 →
- pituitary short stature (E23.0) inherited from E34.3Compare E34.39 vs E23.0 →
- progeria (E34.8) inherited from E34.3Compare E34.39 vs E34.8 →
- renal short stature (N25.0) inherited from E34.3Compare E34.39 vs N25.0 →
- Russell-Silver syndrome (Q87.19) inherited from E34.3Compare E34.39 vs Q87.19 →
- short-limbed stature with immunodeficiency (D82.2) inherited from E34.3Compare E34.39 vs D82.2 →
- short stature (child) (R62.52) inherited from E34.3Compare E34.39 vs R62.52 →
- short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index inherited from E34.3
- short stature NOS (R62.52) inherited from E34.3Compare E34.39 vs R62.52 →
- pseudohypoparathyroidism (E20.1) inherited from E34Compare E34.39 vs E20.1 →
- galactorrhea (N64.3) inherited from E20-E35Compare E34.39 vs N64.3 →
- gynecomastia (N62) inherited from E20-E35Compare E34.39 vs N62 →
Coder workflow for E34.39
MedCoder structured workflow — derived from this code’s own official record
Before you code E34.39
- “Other” (NEC) means the condition is specified in the record but no dedicated code captures it. Confirm the documented form is not one a sibling code names before settling on E34.39; if the record states no specifics at all, the unspecified sibling applies instead. “Other” codes are for documented conditions the classification gives no specific code; “unspecified” codes are for records lacking the detail (Guidelines I.A.9.a, I.A.9.b).
See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →
- E34.39’s title joins a condition with an associated condition or complication. Confirm each component is documented. Where the classification presumes the link through the “with” convention, only a provider statement that the conditions are unrelated defeats it. A combination code is assigned only when it fully identifies the documented conditions; a required second code for the stage, type or manifestation is still reported when the notes ask for it (Guidelines I.B.9, I.A.15).
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E34.39. 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 E34.39’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 E34.39. 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).
- The associated condition or complication
- Whether the associated condition the title names is documented; the “with” convention presumes some links, and a provider statement that the conditions are unrelated defeats it (Guidelines I.A.15).
- Any detail beyond this code’s title
- What the record states that a more specific code would capture — or its absence, which itself supports the unspecified code.
Official instructions as workflow
Excludes1 — check before selecting E34.39(14 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E34.39: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareQ77.4, E45, E23.0, E34.8, N25.0, Q87.19
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 E34.39 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).
Documentation: Only one of the components this code’s title joins is documented.
Coding question: Is E34.39 supported?
Path: Review the code for the documented component on its own.
Reason: A combination code is assigned only when it fully identifies the documented conditions; otherwise the documented component takes its own code (Guidelines I.B.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.
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
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
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 E34.39 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: E23 — Hypofunction and other disorders of the pituitary gland (via E34.3.-), R62.52 — Short stature (child) (via E34.3.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 1 Code First instruction: G63 — Polyneuropathy in diseases classified elsewhere (via E34.-).
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 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 clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Other specified and unspecified endocrine disorders).
E34.0 — Carcinoid syndrome, E34.00 — Carcinoid syndrome, unspecified, E34.01 — Carcinoid heart syndrome, E34.09 — Other carcinoid syndrome, E34.1 — Other hypersecretion of intestinal hormones, E34.2 — Ectopic hormone secretion, not elsewhere classified, E34.3 — Short stature due to endocrine disorder, E34.30 — Short stature due to endocrine disorder, unspecified, E34.31 — Constitutional short stature, E34.321 — Primary insulin-like growth factor-1 (IGF-1) deficiency, E34.322 — Insulin-like growth factor-1 (IGF-1) resistance, E34.328 — Other genetic causes of short stature, E34.329 — Unspecified genetic causes of short stature, E34.4 — Constitutional tall stature, E34.50 — Androgen insensitivity syndrome, unspecified, E34.51 — Complete androgen insensitivity syndrome, E34.52 — Partial androgen insensitivity syndrome, E34.8 — Other specified endocrine disorders, E34.9 — Endocrine disorder, unspecified, E35 — Disorders of endocrine glands in diseases classified elsewhere, +83 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main term “Short, shortening, shortness”; these codes share that main term but sit in a different category of the Tabular List.
D82.2 — Immunodeficiency with short-limbed stature (limbed stature, with immunodeficiency), M67.0 — Short Achilles tendon (acquired) (tendon, Achilles), N36.8 — Other specified disorders of urethra (urethra), N88.3 — Incompetence of cervix uteri (cervical, non-gravid uterus), O26.87 — Cervical shortening (cervical), O69.3 — Labor and delivery complicated by short cord (cord, complicating delivery), Q38.1 — Ankyloglossia (frenum, frenulum, linguae), Q38.5 — Congenital malformations of palate, not elsewhere classified (uvula, congenital), Q39.8 — Other congenital malformations of esophagus (esophagus), Q44.5 — Other congenital malformations of bile ducts (cystic duct, congenital), Q52.4 — Other congenital malformations of vagina (vagina), Q65.89 — Other specified congenital deformities of hip (hip, congenital), Q66.89 — Other specified congenital deformities of feet (tendon, Achilles, congenital), Q71.81 — Congenital shortening of upper limb (arm, congenital), Q72.81 — Congenital shortening of lower limb (leg, congenital), Q77.2 — Short rib syndrome (rib syndrome), Q79.8 — Other congenital malformations of musculoskeletal system (tendon, congenital), R06.02 — Shortness of breath (breath), R62.52 — Short stature (child) (stature NEC)
Contextual Map
Every relationship of E34.39 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 E34.39 with these 3 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-fy2027
- E20-E35 — Disorders of other endocrine glands[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Referenced by Excludes1 notes
- E23 — Hypofunction and other disorders of the pituitary gland[Excludes1](via E34.3.-): “short stature due to endocrine disorder (E34.3-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R62.52 — Short stature (child)[Excludes1](via E34.3.-): “short stature due to endocrine disorder (E34.3-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Code First instructions
- G63 — Polyneuropathy in diseases classified elsewhere[Code First](via E34.-): “endocrine disease, except diabetes (E00-E07, E15-E16, E20-E34)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Clinical classification (CCSR)
- END015 — Other specified and unspecified endocrine disorders[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 643 — ENDOCRINE DISORDERS WITH MCC[MS-DRG]: “ENDOCRINE DISORDERS WITH MCC (MDC 10)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 644 — ENDOCRINE DISORDERS WITH CC[MS-DRG]: “ENDOCRINE DISORDERS WITH CC (MDC 10)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 645 — ENDOCRINE DISORDERS WITHOUT CC/MCC[MS-DRG]: “ENDOCRINE DISORDERS WITHOUT CC/MCC (MDC 10)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
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. 5,013 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027
Index entries
- Short, shortening, shortness, stature NEC (child) (hereditary) (idiopathic), due to, endocrine disorder, specified type NEC, due to endocrine disorder[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
Nearest codes (22)
- E34 — Other endocrine disorders[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E34.0 — Carcinoid syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E34.00 — Carcinoid syndrome, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E34.01 — Carcinoid heart syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E34.09 — Other carcinoid syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E34.1 — Other hypersecretion of intestinal hormones[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E34.2 — Ectopic hormone secretion, not elsewhere classified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E34.3 — Short stature due to endocrine disorder[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- and 14 more
Change history
- FY2023 — Added to the code set[Change history]— CMS release files (code change ledger) · icd10cm-fy2023
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 (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.
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
- 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
- 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. "E34.39 — Other short stature due to endocrine disorder." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/e34.39-other-short-stature-due-to-endocrine-disorder
Change history
- FY2023 — October 1, 2022Added to the code setOther short stature due to endocrine disorderFY2023 changes
Nearest Codes in This Family
Official ICD-10-CM classifications closest to E34.39 in its code family, with their registry titles.
- E34.32 — Genetic causes of short stature
- E34.321 — Primary insulin-like growth factor-1 (IGF-1) deficiency
- E34.322 — Insulin-like growth factor-1 (IGF-1) resistance
- E34.328 — Other genetic causes of short stature
- E34.329 — Unspecified genetic causes of short stature
- E34.4 — Constitutional tall stature
- E34.5 — Androgen insensitivity syndrome
- E34.50 — Androgen insensitivity syndrome, unspecified
- E34.51 — Complete androgen insensitivity syndrome
- E34.52 — Partial androgen insensitivity syndrome