2027 ICD-10-CM Diagnosis Code G70.2Congenital and developmental myasthenia

ICD-10-CM Codes›G00–G99›G70-G73›G70

ICD-10-CM G70.2
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

G70.2 is a billable ICD-10-CM diagnosis code for congenital and developmental myasthenia. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 73 through 74. Coders also document this condition as acetylcholine resynthesis deficiency. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Myopathies.

For Medicare Advantage risk adjustment, G70.2 maps to CMS-HCC Category 196 (Myasthenia Gravis without (Acute) Exacerbation and Other Myoneural Disorders) under the V28 model, adding a risk factor of about 0.516 for a community, non-dual, aged beneficiary in payment year 2027.

Code Identity

ICD-10-CM Code
G70.2
Billable Status
Yes — Valid for Submission
Code Describes
Congenital and developmental myasthenia
Short Description
Congenital and developmental myasthenia
Same as the full description in the CMS dataset.
Parent Code
Myasthenia gravis and other myoneural disorders

Code Classification

ChapterG00–G99Diseases of the nervous system
SectionG70-G73Diseases of myoneural junction and muscle
CategoryG70Myasthenia gravis and other myoneural disorders
This CodeG70.2Congenital and developmental myasthenia

Medicare Risk Adjustment (HCC)Billing

G70.2 maps to a payment category in the CMS-HCC model used to risk-adjust Medicare Advantage payments. Weights are the published community factors for payment year 2027.

CMS-HCC V28 Category (Payment Model)
HCC 196— Myasthenia Gravis without (Acute) Exacerbation and Other Myoneural Disorders
Payment HCC · PY 2027 one of 9 ICD-10-CM codes in this category
Risk Adjustment Factor (RAF) Weight
+0.516
community, non-dual, aged · ranges 0.248–0.642 across segments
Hierarchy
Superseded by HCC 195
a more severe related category takes the payment when both are reported
Prior Model (CMS-HCC V24)
HCC 75
V24 retired V28 pays 100% of MA risk scores since PY 2026
Other CMS Models
PACE (CMS-HCC V22): HCC 75 · ESRD (V21): HCC 75 · ESRD (V24): HCC 75
ESRD V21 weights: 0.059 dialysis, 0.284–0.323 functioning graft · ESRD V24 weights: 0.074 dialysis, 0.344–0.599 functioning graft
Part D (RxHCC)
RxHCC 153 — Myasthenia Gravis and Other Myoneural Disorders
also risk-adjusts in the Part D prescription drug model (V08)

Source: CMS Payment Year 2027 risk adjustment mappings and model software. Weights are relative factors, not dollar amounts; a beneficiary's total RAF also includes demographics and interactions. Browse all CMS-HCC categories.

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Acetylcholine resynthesis deficiency
  • Amyotonia congenita
  • Congenital end-plate acetylcholine receptor deficiency
  • Congenital myasthenic syndrome
  • Congenital myasthenic syndrome with glycosylation defect due to ALG14 UDP-N-acetylglucosaminyltransferase subunit gene mutation
  • Familial infantile myasthenia
  • Genetically determined myasthenia
  • Myasthenia gravis, juvenile form
  • Myasthenic syndrome due to another disorder
  • Pseudomyopathic myasthenia

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to G70.2: its own notes plus those printed at G70 and Chapter 6. A note printed at a category, block or chapter applies to every code under it.

Excludes1

Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.

From G70 Myasthenia gravis and other myoneural disorders applies to 8 codes

Excludes2

Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.

From Chapter 6 (G00-G99) Diseases of the nervous system applies to 700 codes
  • certain conditions originating in the perinatal period (P04-P96)
  • certain infectious and parasitic diseases (A00-B99)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

Source: CMS ICD-10-CM Tabular List. How to read instructional notes.

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR NVS018
Myopathies
Default principal diagnosis: inpatient Yes · outpatient Yes

Patient EducationClinical

Myasthenia Gravis

Myasthenia gravis, sometimes called MG, is a chronic (long-lasting) disease that causes weakness in your voluntary muscles. The voluntary muscles are the ones that you can control. They include the muscles you use for:

The full article covers:

  • What is myasthenia gravis?
  • What causes myasthenia gravis?
  • Who is more likely to develop myasthenia gravis?
  • What are the symptoms of myasthenia gravis?
  • How is myasthenia gravis diagnosed?
  • What are the treatments for myasthenia gravis?

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert G70.2 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
358.8 Myoneural disorders NEC
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2026No changes
FY 2027CurrentCurrent code set, no changesEffective October 1, 2026 through September 30, 2027.

Questions About G70.2Overview

What is the ICD-10 code for congenital and developmental myasthenia?

The ICD-10-CM code for congenital and developmental myasthenia is G70.2 (sometimes written as G702). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is G70.2 (Myasthenia gravis and other myoneural disorders) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report congenital and developmental myasthenia on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

What MS-DRG does G70.2 group to?

When congenital and developmental myasthenia is the principal diagnosis on an inpatient stay, it groups to MS-DRG 74, 73, with relative weights from 1.0172 to 1.5773 depending on complications. Higher weights mean higher Medicare reimbursement.

Can G70.2 be reported with A05.1?

Not as a rule. The Excludes1 note at G70, which applies to G70.2, lists "botulism (A05.1, A48.51-A48.52)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).

What is the ICD-9 equivalent of G70.2?

Under the General Equivalence Mappings, congenital and developmental myasthenia converts to ICD-9-CM 358.8 (myoneural disorders NEC). The mapping is approximate, so confirm the match fits the documentation.

What HCC is G70.2?

G70.2 (congenital and developmental myasthenia) maps to CMS-HCC Category 196 (Myasthenia Gravis without (Acute) Exacerbation and Other Myoneural Disorders), commonly written as HCC 196, in the CMS-HCC V28 model used for Medicare Advantage risk adjustment in payment year 2027. It mapped to HCC 75 under the retired V24 model. It also maps in the PACE (CMS-HCC V22), ESRD (V21), and ESRD (V24) models. In the Part D prescription drug model it maps to RxHCC 153.

Does G70.2 risk-adjust for Medicare Advantage payment?

Yes. When documented and reported on a Medicare Advantage encounter, G70.2 adds a risk adjustment factor of about 0.516 to the beneficiary's RAF score for a community, non-dual, aged enrollee (published V28 weights range from 0.248 to 0.642 depending on the payment segment). A more severe related category (HCC 195) supersedes it when both are reported. See the full factor table on the HCC 196 category page.