| CIM11 |
8A43.2 |
Single transverse myelitis aquaporin-4 antibody positive
|
|
| CIM11 |
8A43.3 |
Recurrent transverse myelitis aquaporin-4 antibody positive
|
|
| CIM11 |
8A43.4 |
Single optic neuritis aquaporin-4 antibody positive
|
|
| CIM11 |
8A43.5 |
Recurrent optic neuritis aquaporin-4 antibody positive
|
|
| CIM11 |
8A44 |
Leukodystrophies
|
|
| CIM11 |
8A44.0 |
Pelizaeus-Merzbacher disease
|
|
| CIM11 |
8A44.1 |
Adrenoleukodystrophy
|
|
| CIM11 |
8A44.2 |
Alexander disease
|
|
| CIM11 |
8A44.3 |
Certain specified leukodystrophies
|
|
| CIM11 |
8A44.4 |
Krabbe disease
|
|
| CIM11 |
8A45 |
Secondary white matter disorders
|
|
| CIM11 |
8A45.0 |
White matter disorders due to infections
|
|
| CIM11 |
8A45.00 |
Human T-cell lymphotropic virus-associated myelopathy
|
|
| CIM11 |
8A45.01 |
Subacute sclerosing panencephalitis
|
|
| CIM11 |
8A45.02 |
Progressive multifocal leukoencephalopathy
|
|
| CIM11 |
8A45.1 |
White matter disorders due to toxicity
|
|
| CIM11 |
8A45.2 |
White matter disorders due to vascular abnormality or ischemia
|
|
| CIM11 |
8A45.20 |
White matter disorder due to CADASIL
|
|
| CIM11 |
8A45.21 |
Subacute necrotising myelitis
|
|
| CIM11 |
8A45.3 |
White matter disorders due to nutritional deficiency
|
|
| CIM11 |
8A45.30 |
White matter disorder due to vitamin B12 deficiency
|
|
| CIM11 |
8A45.31 |
Central pontine myelinolysis
|
|
| CIM11 |
8A45.4 |
White matter disorders due to certain specified systemic disease
|
|
| CIM11 |
8A45.40 |
Demyelination due to sarcoidosis
|
|
| CIM11 |
8A45.41 |
Demyelination due to systemic lupus erythematosus
|
|
| CIM11 |
8A45.42 |
Demyelination due to Sjögren disease
|
|
| CIM11 |
8A45.43 |
Demyelination due to Behcet disease
|
|
| CIM11 |
8A45.44 |
Demyelination due to systemic vasculitis
|
|
| CIM11 |
8A45.45 |
Demyelination due to mitochondrial disease
|
|
| CIM11 |
8A46 |
Central demyelination of corpus callosum
|
|
| CIM11 |
8A60 |
Epilepsy due to structural or metabolic conditions or diseases
|
|
| CIM11 |
8A60.0 |
Epilepsy due to prenatal or perinatal brain insults
|
|
| CIM11 |
8A60.00 |
Epilepsy due to prenatal or perinatal vascular insults
|
|
| CIM11 |
8A60.01 |
Epilepsy due to neonatal hypoxic ischemic encephalopathy
|
|
| CIM11 |
8A60.1 |
Epilepsy due to cerebrovascular disorders
|
|
| CIM11 |
8A60.2 |
Epilepsy due to degenerative brain disorders
|
|
| CIM11 |
8A60.3 |
Epilepsy due to dementias
|
|
| CIM11 |
8A60.4 |
Epilepsy due to central nervous system infections or infestations
|
|
| CIM11 |
8A60.5 |
Epilepsy due to injuries to the head
|
|
| CIM11 |
8A60.6 |
Epilepsy due to tumours of the nervous system
|
|
| CIM11 |
8A60.7 |
Epilepsy with mesial temporal sclerosis
|
|
| CIM11 |
8A60.8 |
Epilepsy due to immune disorders
|
|
| CIM11 |
8A60.9 |
Epilepsy due to abnormalities of brain development
|
|
| CIM11 |
8A60.A |
Epilepsy due to genetic syndromes with widespread or progressive effects
|
|
| CIM11 |
8A60.B |
Epilepsy due to multiple sclerosis or other demyelinating disorders
|
|
| CIM11 |
8A61 |
Genetic or presumed genetic syndromes primarily expressed as epilepsy
|
|
| CIM11 |
8A61.0 |
Genetic epileptic syndromes with neonatal onset
|
|
| CIM11 |
8A61.00 |
Pyridoxal dependent epilepsy
|
|
| CIM11 |
8A61.1 |
Genetic epileptic syndromes with onset in infancy
|
|
| CIM11 |
8A61.10 |
Benign familial infantile epilepsy
|
|