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 v07.1.26.

OASIS-E2 v1.00.0 · ingested 2026-04-26

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.

Every code in G70-G73

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

CodeDescriptionClinical groupPrimary position
G7000Myasthenia gravis without (acute) exacerbationBAccepted
G7001Myasthenia gravis with (acute) exacerbationBAccepted
G701Toxic myoneural disordersNoneCannot group
G702Congenital and developmental myastheniaBAccepted
G7080Lambert-Eaton syndrome, unspecifiedBAccepted
G7081Lambert-Eaton syndrome in disease classified elsewhereNoneCannot group
G7089Other specified myoneural disordersBAccepted
G709Myoneural disorder, unspecifiedNoneCannot group
G7100Muscular dystrophy, unspecifiedBAccepted
G7101Duchenne or Becker muscular dystrophyBAccepted
G7102Facioscapulohumeral muscular dystrophyBAccepted
G71031Autosomal dominant limb girdle muscular dystrophyBAccepted
G71032Autosom recess limb girdle musc dyst d/t calpain-3 dysfnctBAccepted
G71033Limb girdle muscular dystrophy due to dysferlin dysfunctionBAccepted
G710340Limb girdle musc dyst due to sarcoglycan dysfnct, unspBAccepted
G710341Limb girdle musc dyst due to alpha sarcoglycan dysfunctionBAccepted
G710342Limb girdle musc dyst due to beta sarcoglycan dysfunctionBAccepted
G710349Limb girdle musc dyst due to other sarcoglycan dysfunctionBAccepted
G71035Limb girdle musc dyst due to anoctamin-5 dysfunctionBAccepted
G71036Limb girdle musc dyst due to fukutin related protein dysfnctBAccepted
G71038Other limb girdle muscular dystrophyBAccepted
G71039Limb girdle muscular dystrophy, unspecifiedBAccepted
G7109Other specified muscular dystrophiesBAccepted
G7111Myotonic muscular dystrophyBAccepted
G7112Myotonia congenitaBAccepted
G7113Myotonic chondrodystrophyBAccepted
G7114Drug induced myotoniaBAccepted
G7119Other specified myotonic disordersBAccepted
G7120Congenital myopathy, unspecifiedBAccepted
G7121Nemaline myopathyBAccepted
G71220X-linked myotubular myopathyBAccepted
G71228Other centronuclear myopathyBAccepted
G7129Other congenital myopathyBAccepted
G713Mitochondrial myopathy, not elsewhere classifiedBAccepted
G718Other primary disorders of musclesBAccepted
G719Primary disorder of muscle, unspecifiedNoneCannot group
G720Drug-induced myopathyBAccepted
G721Alcoholic myopathyBAccepted
G722Myopathy due to other toxic agentsNoneCannot group
G723Periodic paralysisBAccepted
G7241Inclusion body myositis [IBM]BAccepted
G7249Oth inflammatory and immune myopathies, NECBAccepted
G7281Critical illness myopathyBAccepted
G7289Other specified myopathiesBAccepted
G729Myopathy, unspecifiedBAccepted
G731Lambert-Eaton syndrome in neoplastic diseaseNoneNot accepted
G733Myasthenic syndromes in other diseases classified elsewhereNoneCannot group
G737Myopathy in diseases classified elsewhereNoneCannot group

Source: CMS HH PPS Grouper Software v07.1.26, effective 2026-04-01. 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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