October 1 update. Our PDGM and ICD-10 tools now use the FY2027 code set: 190 codes added, 30 deleted, and no existing code changed clinical group.

See what changed

ICD-10 · PDGM grouping

G70-G73 — Diseases of myoneural junction and muscle

Every ICD-10-CM code in this range and the PDGM clinical group CMS assigns to it, read from the CMS grouper crosswalk v07.2.26.

ICD-10-CM FY2027 · CMS grouper v07.2.26

Codes in range

48

No clinical group

8

A period cannot be grouped from these.

Barred as primary

1

CMS rejects these in the primary position.

Where these codes group

40 of the 48 codes in G70-G73 group to Neuro Rehabilitation. A further 8 are assigned no clinical group at all, which means a 30-day period cannot be grouped from them.

Code families in G70-G73

One page per three-character family: every code in it, whether it can lead a claim, its clinical group and comorbidity subgroup.

Every code in G70-G73

Descriptions are CMS’s own, abbreviated as CMS abbreviates them.

CodeDescriptionClinical groupPrimary position
G7000Myasthenia gravis without (acute) exacerbationBCan lead a claim
G7001Myasthenia gravis with (acute) exacerbationBCan lead a claim
G701Toxic myoneural disordersNoneCannot lead a claim
G702Congenital and developmental myastheniaBCan lead a claim
G7080Lambert-Eaton syndrome, unspecifiedBCan lead a claim
G7081Lambert-Eaton syndrome in disease classified elsewhereNoneCannot lead a claim
G7089Other specified myoneural disordersBCan lead a claim
G709Myoneural disorder, unspecifiedNoneCannot lead a claim
G7100Muscular dystrophy, unspecifiedBCan lead a claim
G7101Duchenne or Becker muscular dystrophyBCan lead a claim
G7102Facioscapulohumeral muscular dystrophyBCan lead a claim
G71031Autosomal dominant limb girdle muscular dystrophyBCan lead a claim
G71032Autosom recess limb girdle musc dyst d/t calpain-3 dysfnctBCan lead a claim
G71033Limb girdle muscular dystrophy due to dysferlin dysfunctionBCan lead a claim
G710340Limb girdle musc dyst due to sarcoglycan dysfnct, unspBCan lead a claim
G710341Limb girdle musc dyst due to alpha sarcoglycan dysfunctionBCan lead a claim
G710342Limb girdle musc dyst due to beta sarcoglycan dysfunctionBCan lead a claim
G710349Limb girdle musc dyst due to other sarcoglycan dysfunctionBCan lead a claim
G71035Limb girdle musc dyst due to anoctamin-5 dysfunctionBCan lead a claim
G71036Limb girdle musc dyst due to fukutin related protein dysfnctBCan lead a claim
G71038Other limb girdle muscular dystrophyBCan lead a claim
G71039Limb girdle muscular dystrophy, unspecifiedBCan lead a claim
G7109Other specified muscular dystrophiesBCan lead a claim
G7111Myotonic muscular dystrophyBCan lead a claim
G7112Myotonia congenitaBCan lead a claim
G7113Myotonic chondrodystrophyBCan lead a claim
G7114Drug induced myotoniaBCan lead a claim
G7119Other specified myotonic disordersBCan lead a claim
G7120Congenital myopathy, unspecifiedBCan lead a claim
G7121Nemaline myopathyBCan lead a claim
G71220X-linked myotubular myopathyBCan lead a claim
G71228Other centronuclear myopathyBCan lead a claim
G7129Other congenital myopathyBCan lead a claim
G713Mitochondrial myopathy, not elsewhere classifiedBCan lead a claim
G718Other primary disorders of musclesBCan lead a claim
G719Primary disorder of muscle, unspecifiedNoneCannot lead a claim
G720Drug-induced myopathyBCan lead a claim
G721Alcoholic myopathyBCan lead a claim
G722Myopathy due to other toxic agentsNoneCannot lead a claim
G723Periodic paralysisBCan lead a claim
G7241Inclusion body myositis [IBM]BCan lead a claim
G7249Oth inflammatory and immune myopathies, NECBCan lead a claim
G7281Critical illness myopathyBCan lead a claim
G7289Other specified myopathiesBCan lead a claim
G729Myopathy, unspecifiedBCan lead a claim
G731Lambert-Eaton syndrome in neoplastic diseaseNoneCannot lead a claim
G733Myasthenic syndromes in other diseases classified elsewhereNoneCannot lead a claim
G737Myopathy in diseases classified elsewhereNoneCannot lead a claim

Source: CMS HH PPS Grouper Software v07.2.26, effective 2026-10-01. This is the crosswalk Medicare runs a claim through. Grouping also depends on admission source, timing, the OASIS functional items and the rest of the diagnosis list.

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