ICD-10-CM › G

ICD-10-CM codes starting with G

932 codes, page 7 of 10. Every code ever valid for billing is listed, including those now retired.

CodeDescriptionStatus
G57.53 Tarsal tunnel syndrome, bilateral lower limbs Valid
G57.6 Lesion of plantar nerve Not billable
G57.60 Lesion of plantar nerve, unspecified lower limb Valid
G57.61 Lesion of plantar nerve, right lower limb Valid
G57.62 Lesion of plantar nerve, left lower limb Valid
G57.63 Lesion of plantar nerve, bilateral lower limbs Valid
G57.7 Causalgia of lower limb Not billable
G57.70 Causalgia of unspecified lower limb Valid
G57.71 Causalgia of right lower limb Valid
G57.72 Causalgia of left lower limb Valid
G57.73 Causalgia of bilateral lower limbs Valid
G57.8 Other specified mononeuropathies of lower limb Not billable
G57.80 Other specified mononeuropathies of unspecified lower limb Valid
G57.81 Other specified mononeuropathies of right lower limb Valid
G57.82 Other specified mononeuropathies of left lower limb Valid
G57.83 Other specified mononeuropathies of bilateral lower limbs Valid
G57.9 Unspecified mononeuropathy of lower limb Not billable
G57.90 Unspecified mononeuropathy of unspecified lower limb Valid
G57.91 Unspecified mononeuropathy of right lower limb Valid
G57.92 Unspecified mononeuropathy of left lower limb Valid
G57.93 Unspecified mononeuropathy of bilateral lower limbs Valid
G58 Other mononeuropathies Not billable
G58.0 Intercostal neuropathy Valid
G58.7 Mononeuritis multiplex Valid
G58.8 Other specified mononeuropathies Valid
G58.9 Mononeuropathy, unspecified Valid
G59 Mononeuropathy in diseases classified elsewhere Valid
G60 Hereditary and idiopathic neuropathy Not billable
G60.0 Hereditary motor and sensory neuropathy Valid
G60.1 Refsum's disease Valid
G60.2 Neuropathy in association with hereditary ataxia Valid
G60.3 Idiopathic progressive neuropathy Valid
G60.8 Other hereditary and idiopathic neuropathies Valid
G60.9 Hereditary and idiopathic neuropathy, unspecified Valid
G61 Inflammatory polyneuropathy Not billable
G61.0 Guillain-Barre syndrome Valid
G61.1 Serum neuropathy Valid
G61.8 Other inflammatory polyneuropathies Not billable
G61.81 Chronic inflammatory demyelinating polyneuritis Valid
G61.82 Multifocal motor neuropathy Valid
G61.89 Other inflammatory polyneuropathies Valid
G61.9 Inflammatory polyneuropathy, unspecified Valid
G62 Other and unspecified polyneuropathies Not billable
G62.0 Drug-induced polyneuropathy Valid
G62.1 Alcoholic polyneuropathy Valid
G62.2 Polyneuropathy due to other toxic agents Valid
G62.8 Other specified polyneuropathies Not billable
G62.81 Critical illness polyneuropathy Valid
G62.82 Radiation-induced polyneuropathy Valid
G62.89 Other specified polyneuropathies Valid
G62.9 Polyneuropathy, unspecified Valid
G63 Polyneuropathy in diseases classified elsewhere Valid
G64 Other disorders of peripheral nervous system Valid
G65 Sequelae of inflammatory and toxic polyneuropathies Not billable
G65.0 Sequelae of Guillain-Barre syndrome Valid
G65.1 Sequelae of other inflammatory polyneuropathy Valid
G65.2 Sequelae of toxic polyneuropathy Valid
G70 Myasthenia gravis and other myoneural disorders Not billable
G70.0 Myasthenia gravis Not billable
G70.00 Myasthenia gravis without (acute) exacerbation Valid
G70.01 Myasthenia gravis with (acute) exacerbation Valid
G70.1 Toxic myoneural disorders Valid
G70.2 Congenital and developmental myasthenia Valid
G70.8 Other specified myoneural disorders Not billable
G70.80 Lambert-Eaton syndrome, unspecified Valid
G70.81 Lambert-Eaton syndrome in disease classified elsewhere Valid
G70.89 Other specified myoneural disorders Valid
G70.9 Myoneural disorder, unspecified Valid
G71 Primary disorders of muscles Not billable
G71.0 Muscular dystrophy Not billable
G71.00 Muscular dystrophy, unspecified Valid
G71.01 Duchenne or Becker muscular dystrophy Valid
G71.02 Facioscapulohumeral muscular dystrophy Valid
G71.03 Limb girdle muscular dystrophies Not billable
G71.031 Autosomal dominant limb girdle muscular dystrophy Valid
G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction Valid
G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction Valid
G71.034 Limb girdle muscular dystrophy due to sarcoglycan dysfunction Not billable
G71.0340 Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified Valid
G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction Valid
G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction Valid
G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction Valid
G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction Valid
G71.036 Limb girdle muscular dystrophy due to fukutin related protein dysfunction Valid
G71.038 Other limb girdle muscular dystrophy Valid
G71.039 Limb girdle muscular dystrophy, unspecified Valid
G71.09 Other specified muscular dystrophies Valid
G71.1 Myotonic disorders Not billable
G71.11 Myotonic muscular dystrophy Valid
G71.12 Myotonia congenita Valid
G71.13 Myotonic chondrodystrophy Valid
G71.14 Drug induced myotonia Valid
G71.19 Other specified myotonic disorders Valid
G71.2 Congenital myopathies Not billable
G71.20 Congenital myopathy, unspecified Valid
G71.21 Nemaline myopathy Valid
G71.22 Centronuclear myopathy Not billable
G71.220 X-linked myotubular myopathy Valid
G71.228 Other centronuclear myopathy Valid
G71.29 Other congenital myopathy Valid
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