FREQUENTL 1 O - BioReference
FREQUENTLY USED ICD10 CODES
NEUROLOGY
Delay/ID
Speech & Language Disorders
F70 F71 F79 G31.84 F84.0 F84.9 Q99.2 F90.1 F80.2
F80.9
F95.2
R47.1
DEVELOPMENTAL
Mild intellectual disabilities Moderate intellectual disabilities Unspecified intellectual disabilities Mild cognitive impairment, so stated
R62.0 F81.9 R62.51 F82
Delayed milestone in childhood Developmental disorder of scholastic skills, unspecified Failure to thrive (child) Specific developmental disorder of motor function
Autistic disorder Pervasive developmental disorder, unspecified Fragile X syndrome
F88 R62.50 F89
Other disorders of psychological development Unspecified lack of expected normal physiological development in childhood Unspecified disorder of psychological development
Attention-deficit hyperactivity disorder, predominantly hyperactive type
Mixed receptive-expressive language disorder
Developmental disorder of speech and language, unspecified
Tourette's disorder
Dysarthria and anarthria
Q02 Q75.3 R90.82 E75.25 I67.850 E75.29 R90.89
R93.0
CNS-BRAIN
Microcephaly
Q04.5 Megalencephaly
Macrocephaly
White matter disease, unspecified
Metachromatic leukodystrophy
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Other sphingolipidosis
Other abnormal findings on diagnostic imaging of central nervous system
Abnormal findings on diagnostic imaging of skull and head, not elsewhere classified
Q03.9 Congenital hydrocephalus, unspecified
Other Brain malformations Hydrocephalus Imaging Leukodystrophy Size
G91.9 Hydrocephalus, unspecified
Q28.3 Q04.0
Other malformations of cerebral vessels Congenital malformations of corpus callosum
Q04.2 Q04.9
Holoprosencephaly Congenital malformation of brain, unspecified
Q03.1
Q07.8 G90.9 I63.9
Atresia of foramina of Magendie and Luschka
Other specified congenital malformations of the nervous system Disorder of the autonomic nervous system, unspecified Cerebral infarction, unspecified
Q04.8 Other specified congenital malformations of brain
Q04.3 G93.89
Other reduction deformities of brain Other specified disorders of the brain
This is not a comprehensive list of ICD-10 codes. There are more codes available. Please visit for a complete list of codes.
This list is intended to assist ordering physicians in providing ICD-10 Diagnosis Codes as required by Medicare and other Insurers. It includes the most commonly found out-patient diagnoses (generally without complications), but is not complete.
This list was compiled from the 2019 ICD-10-CM [effective 10/1/18], as well as the Medicare Regulations and Manuals issued or authorized by the Centers for Medicaid and Medicare Services. An ICD-10-CM book should be used as a complete reference. The ultimate responsibility for correct coding belongs to the ordering physician.
200822 V1 07/19 INFORMATION CURRENT AS OF 07/19
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FREQUENTLY USED ICD10 CODES
NEUROLOGY
Intractable
G40.311 G40.411 G40.911 G40.823 G40.111
G40.211
G40.011 G40.813 G40.A11 G40.B11
G40.301 G40.401 G40.901 G40.822 G40.101
G40.201
G40.001 G40.811 G40.A01 G40.B01
P90 R56.9 G93.40
EPILEPSY
With Status Epilepticus
Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus
G40.319
Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus
G40.419
Epilepsy, unspecified, intractable, with status epilepticus
G40.919
Epileptic spasms, intractable, with status epilepticus
G40.824
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus
G40.119
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus
G40.219
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus
G40.019
Lennox-Gastaut syndrome, intractable, with status epilepticus
G40.814
Absence epileptic syndrome, intractable, with status epilepticus
G40.A19
Juvenile myoclonic epilepsy, intractable, with status epilepticus
G40.B19
With Status Epilepticus
Generlized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40.309
Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40.409
Epilepsy, unspecified, not intractable, with status epilepticus
G40.909
Epileptic spasms, not intractable, with status epilepticus
G40.821
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus
G40.109
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus
G40.209
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus
G40.009
Lennox-Gastaut syndrome, not intractable, with status epilepticus
G40.812
Absence epileptic syndrome, not intractable, with status epilepticus
G40.802
Juvenile myoclonic epilepsy, not intractable, with status epilepticus
G40.A09
G40.B09
Convulsions of newborn
G93.49
Unspecified convulsions
G40.89
Encephalopathy, unspecified
Without Status Epilepticus
Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus
Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus
Epilepsy, unspecified, intractable, without status epilepticus
Epileptic spasms, intractable, without status epilepticus
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus
Lennox-Gastaut syndrome, intractable, without status epilepticus
Absence epileptic syndrome, intractable, without status epilepticus
Juvenile myoclonic epilepsy, intractable, without status epilepticus
Without Status Epilepticus
Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus
Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus
Epilepsy, unspecified, not intractable, without status epilepticus
Epileptic spasms, not intractable, without status epilepticus
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus
Lennox-Gastaut syndrome, not intractable, without status epilepticus
Other epilepsy, not intractable, without status epilepticus
Absence epileptic syndrome, not intractable, without status epilepticus
Juvenile myoclonic epilepsy, not intractable, without status epilepticus
Other encephalopathy
Other seizures
Not Intractable
Other
This is not a comprehensive list of ICD-10 codes. There are more codes available. Please visit for a complete list of codes.
This list is intended to assist ordering physicians in providing ICD-10 Diagnosis Codes as required by Medicare and other Insurers. It includes the most commonly found out-patient diagnoses (generally without complications), but is not complete.
This list was compiled from the 2019 ICD-10-CM [effective 10/1/18], as well as the Medicare Regulations and Manuals issued or authorized by the Centers for Medicaid and Medicare Services. An ICD-10-CM book should be used as a complete reference. The ultimate responsibility for correct coding belongs to the ordering physician.
200822 V1 07/19 INFORMATION CURRENT AS OF 07/19
Page 2
FREQUENTLY USED ICD10 CODES
NEUROLOGY
G30.0 G30.9 G12.21 R47.01 G31.9
Alzheimer's disease with early onset Alzheimer's disease, unspecified Amyotrophic lateral sclerosis Aphasia Degenerative disease of nervous system, unspecified
NEURODEGENERATIVE
G31.09 Other frontotemporal dementia
G20
Parkinson's disease
F03.91 Unspecified dementia with behavioral disturbance
F03.90 Unspecified dementia without behavioral disturbance
Neuropathy
Myopathy
Sensory Other neuromuscular
MUSCULOSKELETAL
G60.0 Hereditary motor and sensory neuropathy
G60.9 Hereditary and idiopathic neuropathy, unspecified
G60.3 Idiopathic progressive neuropathy
G61.81 Chronic inflammatory demyelinating polyneuritis
G60.8 Other hereditary and idiopathic neuropathies
G62.9 Polyneuropathy, unspecified
G12.20 Motor neuron disease, unspecified
G12.0 Infantile spinal muscular atrophy, type 1
G71.01 Duchenne or Becker muscular dystrophy
G71.11 Myotonic muscular dystrophy
G71.2 Congenital myopathies
G71.3 Mitochondrial myopathy, not elsewhere classified (Leber's disease, Leigh's encephalopathy, Kearns-Sayre syndrome, mitochondrial metabolism disorders)
G71.09 Other specified muscular dystrophies (Limb-Girdle, Ocular, Oculopharyngeal, scapuloperoneal, congenital)
M62.89 Other specified disorders of muscle
G72.9 Myopathy, unspecified
R25.2 Cramp and spasm
M62.81 Muscle weakness (generalized)
R26.89 Other abnormalities of gait and mobility
R94.131 Abnormal electromyogram (EMG)
R26.9 Unspecified abnormalities of gait and mobility
P94.2 Congenital hypotonia
R29.898 Other symptoms and signs involving the musculoskeletal system
G70.2 Congenital and developmental myasthenia
R53.1 Weakness
G70.9 Myoneural disorder, unspecified
M79.673 Pain in unspecified foot
M79.643 Pain in unspecified hand
M79.641 Pain in right hand
R20.2 Paresthesia of skin
M79.642 Pain in left hand
M79.671 Pain in right foot
M79.606 Pain in leg, unspecified
M79.672 Pain in left foot
Q87.1 Congenital malformation syndromes predominately associated with short stature
Q66.7 Congenital pes cavus
R62.52 Short stature (child)
Q67.5 Congenital deformity of the spine (scolisis/kyphoscholsis)
M41.9 Scoliosis, unspecified
G95.9 Disease of spinal cord, unspecified
Skeletal
This is not a comprehensive list of ICD-10 codes. There are more codes available. Please visit for a complete list of codes.
This list is intended to assist ordering physicians in providing ICD-10 Diagnosis Codes as required by Medicare and other Insurers. It includes the most commonly found out-patient diagnoses (generally without complications), but is not complete.
This list was compiled from the 2019 ICD-10-CM [effective 10/1/18], as well as the Medicare Regulations and Manuals issued or authorized by the Centers for Medicaid and Medicare Services. An ICD-10-CM book should be used as a complete reference. The ultimate responsibility for correct coding belongs to the ordering physician.
200822 V1 07/19 INFORMATION CURRENT AS OF 07/19
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FREQUENTLY USED ICD10 CODES
NEUROLOGY
Other Dystonia Ataxia Cerebral Palsy
G80.8 G80.9 G80.1 G80.0 G11.1 G11.2 G11.8 G24.9
G24.8 R26.1 G11.4 R25.1
Other cerebral palsy Cerebral palsy, unspecified Spastic diplegic cerebral palsy Spastic quadriplegic cerebral palsy Early-onset cerebellar ataxia Late-onset cerebellar ataxia Other hereditary ataxias Dystonia, unspecified
Other dystonia Paralytic gait Hereditary spastic paraplegia Tremor, unspecified
MOVEMENT
G80.2 G82.50 G82.20
Spastic hemiplegic cerebral palsy Quadriplegia, unspecified Paraplegia, unspecified
G11.9 G32.81 R27.0
Hereditary ataxia, unspecified Cerebellar ataxia in diseases classified elsewhere Ataxia, unspecified
G83.9 F98.4
Paralytic syndrome, unspecified Stereotyped movement disorders
R74.8 D17.71 D21.9 Q18.9 Q87.3 L81.9 P08.0
Abnormal levels of other serum enzymes Benign lipomatous neoplasm of kidney Benign neoplasm of connective and other soft tissue, unspecified Congenital malformation of face and neck, unspecified Congenital malformation syndromes involving early overgrowth Disorder of pigmentation, unspecified Exceptionally large newborn baby
OTHER
Q38.2 Q89.7 P05.10 E28.39 Q85.1 Z13.71 O28.3
Macroglossia Multiple congenital malformations, not elsewhere classified Newborn small for gestational age, unspecified weight Other primary ovarian failure Tuberous sclerosis Encounter for nonprocreative screening for genetic disease carrier status Abnormal ultrasonic finding on antenatal screening of mother
Z82.0 Z81.8 Z84.81
FAMILY HISTORY
Family history of epilepsy and other diseases of the nervous system Family history of other mental and behavioral disorders Family history of carrier of genetic disease
This is not a comprehensive list of ICD-10 codes. There are more codes available. Please visit for a complete list of codes.
This list is intended to assist ordering physicians in providing ICD-10 Diagnosis Codes as required by Medicare and other Insurers. It includes the most commonly found out-patient diagnoses (generally without complications), but is not complete.
This list was compiled from the 2019 ICD-10-CM [effective 10/1/18], as well as the Medicare Regulations and Manuals issued or authorized by the Centers for Medicaid and Medicare Services. An ICD-10-CM book should be used as a complete reference. The ultimate responsibility for correct coding belongs to the ordering physician.
200822 V1 07/19 INFORMATION CURRENT AS OF 07/19
Page 4
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