Risk-adjusting code directory
Page 11 of 33
Codes 2,501 through 2,750 of 8,016 billable ICD-10-CM codes with V28 HCC mapping.
G36.9
Acute disseminated demyelination, unspecified
198
G37.0
Diffuse sclerosis of central nervous system
198
G37.1
Central demyelination of corpus callosum
198
G37.2
Central pontine myelinolysis
198
G37.3
Acute transverse myelitis in demyelinating disease of central nervous system
182
G37.4
Subacute necrotizing myelitis of central nervous system
182
G37.5
Concentric sclerosis [Balo] of central nervous system
198
G37.81
Myelin oligodendrocyte glycoprotein antibody disease
198
G37.89
Other specified demyelinating diseases of central nervous system
198
G37.9
Demyelinating disease of central nervous system, unspecified
198
G40.001
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus
201
G40.009
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus
201
G40.011
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus
201
G40.019
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus
201
G40.101
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus
201
G40.109
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus
201
G40.111
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus
201
G40.119
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus
201
G40.201
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus
201
G40.209
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus
201
G40.211
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus
201
G40.219
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus
201
G40.301
Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus
201
G40.309
Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus
201
G40.311
Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus
201
G40.319
Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus
201
G40.401
Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus
201
G40.409
Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus
201
G40.411
Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus
201
G40.419
Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus
201
G40.42
Cyclin-Dependent Kinase-Like 5 Deficiency Disorder
201
G40.501
Epileptic seizures related to external causes, not intractable, with status epilepticus
201
G40.509
Epileptic seizures related to external causes, not intractable, without status epilepticus
201
G40.801
Other epilepsy, not intractable, with status epilepticus
201
G40.802
Other epilepsy, not intractable, without status epilepticus
201
G40.803
Other epilepsy, intractable, with status epilepticus
201
G40.804
Other epilepsy, intractable, without status epilepticus
201
G40.811
Lennox-Gastaut syndrome, not intractable, with status epilepticus
201
G40.812
Lennox-Gastaut syndrome, not intractable, without status epilepticus
201
G40.813
Lennox-Gastaut syndrome, intractable, with status epilepticus
201
G40.814
Lennox-Gastaut syndrome, intractable, without status epilepticus
201
G40.821
Epileptic spasms, not intractable, with status epilepticus
201
G40.822
Epileptic spasms, not intractable, without status epilepticus
201
G40.823
Epileptic spasms, intractable, with status epilepticus
201
G40.824
Epileptic spasms, intractable, without status epilepticus
201
G40.833
Dravet syndrome, intractable, with status epilepticus
201
G40.834
Dravet syndrome, intractable, without status epilepticus
201
G40.841
KCNQ2-related epilepsy, not intractable, with status epilepticus
201
G40.842
KCNQ2-related epilepsy, not intractable, without status epilepticus
201
G40.843
KCNQ2-related epilepsy, intractable, with status epilepticus
201
G40.844
KCNQ2-related epilepsy, intractable, without status epilepticus
201
G40.89
Other seizures
201
G40.901
Epilepsy, unspecified, not intractable, with status epilepticus
201
G40.909
Epilepsy, unspecified, not intractable, without status epilepticus
201
G40.911
Epilepsy, unspecified, intractable, with status epilepticus
201
G40.919
Epilepsy, unspecified, intractable, without status epilepticus
201
G40.A01
Absence epileptic syndrome, not intractable, with status epilepticus
201
G40.A09
Absence epileptic syndrome, not intractable, without status epilepticus
201
G40.A11
Absence epileptic syndrome, intractable, with status epilepticus
201
G40.A19
Absence epileptic syndrome, intractable, without status epilepticus
201
G40.B01
Juvenile myoclonic epilepsy, not intractable, with status epilepticus
201
G40.B09
Juvenile myoclonic epilepsy, not intractable, without status epilepticus
201
G40.B11
Juvenile myoclonic epilepsy, intractable, with status epilepticus
201
G40.B19
Juvenile myoclonic epilepsy, intractable, without status epilepticus
201
G40.C01
Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus
201
G40.C09
Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
201
G40.C11
Lafora progressive myoclonus epilepsy, intractable, with status epilepticus
201
G40.C19
Lafora progressive myoclonus epilepsy, intractable, without status epilepticus
201
G54.6
Phantom limb syndrome with pain
409
G54.7
Phantom limb syndrome without pain
409
G61.81
Chronic inflammatory demyelinating polyneuritis
193
G61.82
Multifocal motor neuropathy
193
G70.00
Myasthenia gravis without (acute) exacerbation
196
G70.01
Myasthenia gravis with (acute) exacerbation
195
G70.1
Toxic myoneural disorders
196
G70.2
Congenital and developmental myasthenia
196
G70.80
Lambert-Eaton syndrome, unspecified
196
G70.81
Lambert-Eaton syndrome in disease classified elsewhere
196
G70.89
Other specified myoneural disorders
196
G70.9
Myoneural disorder, unspecified
196
G71.00
Muscular dystrophy, unspecified
197
G71.01
Duchenne or Becker muscular dystrophy
197
G71.02
Facioscapulohumeral muscular dystrophy
197
G71.031
Autosomal dominant limb girdle muscular dystrophy
197
G71.032
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
197
G71.033
Limb girdle muscular dystrophy due to dysferlin dysfunction
197
G71.0340
Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
197
G71.0341
Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
197
G71.0342
Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
197
G71.0349
Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
197
G71.035
Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
197
G71.036
Limb girdle muscular dystrophy due to fukutin related protein dysfunction
197
G71.038
Other limb girdle muscular dystrophy
197
G71.039
Limb girdle muscular dystrophy, unspecified
197
G71.09
Other specified muscular dystrophies
197
G71.11
Myotonic muscular dystrophy
197
G71.20
Congenital myopathy, unspecified
197
G71.21
Nemaline myopathy
197
G71.220
X-linked myotubular myopathy
197
G71.228
Other centronuclear myopathy
197
G71.29
Other congenital myopathy
197
G72.41
Inclusion body myositis [IBM]
93
G73.1
Lambert-Eaton syndrome in neoplastic disease
196
G73.3
Myasthenic syndromes in other diseases classified elsewhere
196
G80.0
Spastic quadriplegic cerebral palsy
191
G80.1
Spastic diplegic cerebral palsy
192
G80.2
Spastic hemiplegic cerebral palsy
192
G80.3
Athetoid cerebral palsy
192
G80.4
Ataxic cerebral palsy
192
G80.8
Other cerebral palsy
192
G80.9
Cerebral palsy, unspecified
192
G81.00
Flaccid hemiplegia affecting unspecified side
253
G81.01
Flaccid hemiplegia affecting right dominant side
253
G81.02
Flaccid hemiplegia affecting left dominant side
253
G81.03
Flaccid hemiplegia affecting right nondominant side
253
G81.04
Flaccid hemiplegia affecting left nondominant side
253
G81.10
Spastic hemiplegia affecting unspecified side
253
G81.11
Spastic hemiplegia affecting right dominant side
253
G81.12
Spastic hemiplegia affecting left dominant side
253
G81.13
Spastic hemiplegia affecting right nondominant side
253
G81.14
Spastic hemiplegia affecting left nondominant side
253
G81.90
Hemiplegia, unspecified affecting unspecified side
253
G81.91
Hemiplegia, unspecified affecting right dominant side
253
G81.92
Hemiplegia, unspecified affecting left dominant side
253
G81.93
Hemiplegia, unspecified affecting right nondominant side
253
G81.94
Hemiplegia, unspecified affecting left nondominant side
253
G82.20
Paraplegia, unspecified
181
G82.21
Paraplegia, complete
181
G82.22
Paraplegia, incomplete
181
G82.50
Quadriplegia, unspecified
180
G82.51
Quadriplegia, C1-C4 complete
180
G82.52
Quadriplegia, C1-C4 incomplete
180
G82.53
Quadriplegia, C5-C7 complete
180
G82.54
Quadriplegia, C5-C7 incomplete
180
G83.0
Diplegia of upper limbs
254
G83.10
Monoplegia of lower limb affecting unspecified side
254
G83.11
Monoplegia of lower limb affecting right dominant side
254
G83.12
Monoplegia of lower limb affecting left dominant side
254
G83.13
Monoplegia of lower limb affecting right nondominant side
254
G83.14
Monoplegia of lower limb affecting left nondominant side
254
G83.20
Monoplegia of upper limb affecting unspecified side
254
G83.21
Monoplegia of upper limb affecting right dominant side
254
G83.22
Monoplegia of upper limb affecting left dominant side
254
G83.23
Monoplegia of upper limb affecting right nondominant side
254
G83.24
Monoplegia of upper limb affecting left nondominant side
254
G83.30
Monoplegia, unspecified affecting unspecified side
254
G83.31
Monoplegia, unspecified affecting right dominant side
254
G83.32
Monoplegia, unspecified affecting left dominant side
254
G83.33
Monoplegia, unspecified affecting right nondominant side
254
G83.34
Monoplegia, unspecified affecting left nondominant side
254
G83.4
Cauda equina syndrome
182
G83.5
Locked-in state
254
G83.81
Brown-Sequard syndrome
254
G83.82
Anterior cord syndrome
254
G83.83
Posterior cord syndrome
254
G83.84
Todd's paralysis (postepileptic)
254
G83.89
Other specified paralytic syndromes
254
G83.9
Paralytic syndrome, unspecified
254
G90.1
Familial dysautonomia [Riley-Day]
182
G90.3
Multi-system degeneration of the autonomic nervous system
199
G90.B
LMNB1-related autosomal dominant leukodystrophy
200
G91.0
Communicating hydrocephalus
127
G91.1
Obstructive hydrocephalus
127
G91.2
(Idiopathic) normal pressure hydrocephalus
127
G91.3
Post-traumatic hydrocephalus, unspecified
127
G91.4
Hydrocephalus in diseases classified elsewhere
127
G91.8
Other hydrocephalus
127
G91.9
Hydrocephalus, unspecified
127
G93.1
Anoxic brain damage, not elsewhere classified
202
G93.42
Megalencephalic leukoencephalopathy with subcortical cysts
200
G93.43
Leukoencephalopathy with calcifications and cysts
200
G93.44
Adult-onset leukodystrophy with axonal spheroids
200
G93.45
Developmental and epileptic encephalopathy
201
G93.5
Compression of brain
202
G93.6
Cerebral edema
202
G93.7
Reye's syndrome
127
G95.0
Syringomyelia and syringobulbia
182
G95.11
Acute infarction of spinal cord (embolic) (nonembolic)
182
G95.19
Other vascular myelopathies
182
G95.20
Unspecified cord compression
182
G95.29
Other cord compression
182
G95.81
Conus medullaris syndrome
182
G95.89
Other specified diseases of spinal cord
182
G95.9
Disease of spinal cord, unspecified
182
G99.2
Myelopathy in diseases classified elsewhere
182
H34.8110
Central retinal vein occlusion, right eye, with macular edema
298
H34.8111
Central retinal vein occlusion, right eye, with retinal neovascularization
298
H34.8112
Central retinal vein occlusion, right eye, stable
298
H34.8120
Central retinal vein occlusion, left eye, with macular edema
298
H34.8121
Central retinal vein occlusion, left eye, with retinal neovascularization
298
H34.8122
Central retinal vein occlusion, left eye, stable
298
H34.8130
Central retinal vein occlusion, bilateral, with macular edema
298
H34.8131
Central retinal vein occlusion, bilateral, with retinal neovascularization
298
H34.8132
Central retinal vein occlusion, bilateral, stable
298
H34.8190
Central retinal vein occlusion, unspecified eye, with macular edema
298
H34.8191
Central retinal vein occlusion, unspecified eye, with retinal neovascularization
298
H34.8192
Central retinal vein occlusion, unspecified eye, stable
298
H34.8310
Tributary (branch) retinal vein occlusion, right eye, with macular edema
298
H34.8311
Tributary (branch) retinal vein occlusion, right eye, with retinal neovascularization
298
H34.8312
Tributary (branch) retinal vein occlusion, right eye, stable
298
H34.8320
Tributary (branch) retinal vein occlusion, left eye, with macular edema
298
H34.8321
Tributary (branch) retinal vein occlusion, left eye, with retinal neovascularization
298
H34.8322
Tributary (branch) retinal vein occlusion, left eye, stable
298
H34.8330
Tributary (branch) retinal vein occlusion, bilateral, with macular edema
298
H34.8331
Tributary (branch) retinal vein occlusion, bilateral, with retinal neovascularization
298
H34.8332
Tributary (branch) retinal vein occlusion, bilateral, stable
298
H34.8390
Tributary (branch) retinal vein occlusion, unspecified eye, with macular edema
298
H34.8391
Tributary (branch) retinal vein occlusion, unspecified eye, with retinal neovascularization
298
H34.8392
Tributary (branch) retinal vein occlusion, unspecified eye, stable
298
H35.3210
Exudative age-related macular degeneration, right eye, stage unspecified
300
H35.3211
Exudative age-related macular degeneration, right eye, with active choroidal neovascularization
300
H35.3212
Exudative age-related macular degeneration, right eye, with inactive choroidal neovascularization
300
H35.3213
Exudative age-related macular degeneration, right eye, with inactive scar
300
H35.3220
Exudative age-related macular degeneration, left eye, stage unspecified
300
H35.3221
Exudative age-related macular degeneration, left eye, with active choroidal neovascularization
300
H35.3222
Exudative age-related macular degeneration, left eye, with inactive choroidal neovascularization
300
H35.3223
Exudative age-related macular degeneration, left eye, with inactive scar
300
H35.3230
Exudative age-related macular degeneration, bilateral, stage unspecified
300
H35.3231
Exudative age-related macular degeneration, bilateral, with active choroidal neovascularization
300
H35.3232
Exudative age-related macular degeneration, bilateral, with inactive choroidal neovascularization
300
H35.3233
Exudative age-related macular degeneration, bilateral, with inactive scar
300
H35.3290
Exudative age-related macular degeneration, unspecified eye, stage unspecified
300
H35.3291
Exudative age-related macular degeneration, unspecified eye, with active choroidal neovascularization
300
H35.3292
Exudative age-related macular degeneration, unspecified eye, with inactive choroidal neovascularization
300
H35.3293
Exudative age-related macular degeneration, unspecified eye, with inactive scar
300
H36.811
Nonproliferative sickle-cell retinopathy, right eye
108
H36.812
Nonproliferative sickle-cell retinopathy, left eye
108
H36.813
Nonproliferative sickle-cell retinopathy, bilateral
108
H36.819
Nonproliferative sickle-cell retinopathy, unspecified eye
108
H36.821
Proliferative sickle-cell retinopathy, right eye
108,298
H36.822
Proliferative sickle-cell retinopathy, left eye
108,298
H36.823
Proliferative sickle-cell retinopathy, bilateral
108,298
H36.829
Proliferative sickle-cell retinopathy, unspecified eye
108,298
H43.10
Vitreous hemorrhage, unspecified eye
298
H43.11
Vitreous hemorrhage, right eye
298
H43.12
Vitreous hemorrhage, left eye
298
H43.13
Vitreous hemorrhage, bilateral
298
I09.81
Rheumatic heart failure
226
I11.0
Hypertensive heart disease with heart failure
226
I12.0
Hypertensive chronic kidney disease with stage 5 chronic kidney disease or end stage renal disease
326
I13.0
Hypertensive heart and chronic kidney disease with heart failure and stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease
226
I13.11
Hypertensive heart and chronic kidney disease without heart failure, with stage 5 chronic kidney disease, or end stage renal disease
326
I13.2
Hypertensive heart and chronic kidney disease with heart failure and with stage 5 chronic kidney disease, or end stage renal disease
226,326
I20.0
Unstable angina
229
I21.01
ST elevation (STEMI) myocardial infarction involving left main coronary artery
228
I21.02
ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery
228
I21.09
ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall
228
I21.11
ST elevation (STEMI) myocardial infarction involving right coronary artery
228
I21.19
ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall
228
I21.21
ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery
228