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Category
Psychiatry | NeuroPathology | ||||||||||||||||||||||||||||||||||||||||||
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Code
Psychiatry | |||
|---|---|---|---|
| psycode | count | description | psycat |
| 0 | 1784 | Control (No known history of mental disorders): Unknown (insufficient information) | |
| 100 | 1 | Control (No known history of mental disorders): No history of mental disorders (ruled out by structured interview) | Control |
| 200 | 194 | Schizophrenia | Schizo |
| 300 | 24 | Bipolar disorders | Bipolar |
| 400 | 18 | Depression | Depression |
| 500 | 0 | Neurodevelopmental disorders | |
| 501 | 0 | - - - - - - ASD | ASD |
| 502 | 0 | - - - - - - ADHD | ADHD |
| 503 | 9 | - - - - - - MR | MR |
| 600 | 273 | Others | |
NeuroPathology | |||
| npcode | count | description | npcat |
| 0 | 619 | Unknown/Miscellaneous | |
| 10000 | 103 | Control | Control |
| 20000 | 42 | Aging and dementia | |
| 20100 | 165 | - - - - - - Alzheimer disease(AD) | AD |
| 20101 | 0 | - - - - - - - - - - - - Preclinical AD | AD |
| 20102 | 9 | - - - - - - - - - - - - Prodromal AD | AD |
| 20103 | 2 | - - - - - - - - - - - - Sporadic AD | AD |
| 20104 | 0 | - - - - - - - - - - - - Familial AD | AD |
| 20200 | 44 | - - - - - - Lewy body disease (PD/ DLB- pure, common, AD) | LBD |
| 20201 | 4 | - - - - - - - - - - - - Incidental LBD | LBD |
| 20202 | 12 | - - - - - - - - - - - - Preclinical LBD | LBD |
| 20203 | 65 | - - - - - - - - - - - - PD | LBD |
| 20204 | 26 | - - - - - - - - - - - - PDD | LBD |
| 20205 | 25 | - - - - - - - - - - - - DLB-pure | LBD |
| 20206 | 1 | - - - - - - - - - - - - DLB-common | LBD |
| 20207 | 3 | - - - - - - - - - - - - DLB AD form | LBD |
| 20300 | 3 | - - - - - - Pick's disease | Pick |
| 20400 | 84 | - - - - - - Argyrophilic grain dementia (AGD) | |
| 20500 | 79 | - - - - - - NFTD (PART) | |
| 20600 | 97 | - - - - - - Progressive supranuclear palsy | PSP |
| 20700 | 15 | - - - - - - Corticobasal degeneration | CBD |
| 20800 | 10 | - - - - - - hippocampal sclerosis (HS) dementia | |
| 20900 | 5 | - - - - - - Vascular and mixed dementia | |
| 21000 | 5 | - - - - - - FTLD | |
| 21001 | 4 | - - - - - - - - - - - - FTLD-TDP | |
| 21002 | 0 | - - - - - - - - - - - - FTLD with MAPT mutaion | |
| 21003 | 0 | - - - - - - - - - - - - FTLD-FUS | |
| 21100 | 5 | - - - - - - Globular glial tauopathy | |
| 21200 | 19 | - - - - - - Huntington disease | HD |
| 30000 | 3 | Motor Neuron Disease | MND |
| 30100 | 124 | - - - - - - ALS (ALS/ ALSD/ FTLD- MND) | MND |
| 30101 | 44 | - - - - - - - - - - - - ALS | MND |
| 30102 | 5 | - - - - - - - - - - - - ALS-D/ FTLD- MND | MND |
| 30200 | 1 | - - - - - - Spinal muscular atrophy | MND |
| 30300 | 4 | - - - - - - X-linked spinal and bulbar muscular atrophy | MND |
| 40000 | 2 | Spinocerebellar degeneration (ataxia: SCA) | |
| 40100 | 2 | - - - - - - Autosomal dominant SCAs | |
| 40101 | 18 | - - - - - - - - - - - - Dentatorubral pallidoluysian atrophy | DRPLA |
| 40102 | 18 | - - - - - - - - - - - - Machado-Joseph disease/ SCA3 | |
| 40103 | 3 | - - - - - - - - - - - - SCA6 | |
| 40104 | 2 | - - - - - - - - - - - - SCA31 | |
| 40200 | 0 | - - - - - - Autosomal recessive cerebellar ataxias | |
| 40300 | 0 | - - - - - - Sporadic spinocerebellar degeneration | |
| 40301 | 93 | - - - - - - - - - - - - Multiple system atrophy | MSA |
| 50000 | 2 | Demyelinating disease | |
| 50100 | 4 | - - - - - - Multiple sclerosis | MS |
| 50200 | 1 | - - - - - - Neuromyelitis optica | |
| 60000 | 2 | Leukuencephalopathies | |
| 60100 | 2 | - - - - - - HDLS | |
| 60200 | 0 | - - - - - - Nasu-Hakola disease | |
| 60300 | 0 | - - - - - - CADASIL | |
| 60400 | 0 | - - - - - - CARASIL | |
| 60500 | 0 | - - - - - - Vanishing white matter disease | |
| 60600 | 3 | - - - - - - Neuronal intranuclear inclusion disease | |
| 70000 | 14 | Infectious disorders | |
| 70100 | 3 | - - - - - - Bacterial infections | |
| 70101 | 2 | - - - - - - - - - - - - Purulent leptomeningitis | |
| 70102 | 5 | - - - - - - - - - - - - Brain abscess / Microabscess | |
| 70200 | 1 | - - - - - - Mycotic infections | |
| 70300 | 3 | - - - - - - Parasitic infections | |
| 70400 | 2 | - - - - - - Viral infections | |
| 70401 | 2 | - - - - - - - - - - - - Herpes simplex encephalitis | |
| 70402 | 0 | - - - - - - - - - - - - SSPE | |
| 70403 | 1 | - - - - - - - - - - - - PML | |
| 70404 | 0 | - - - - - - - - - - - - AIDS / HIV | |
| 70405 | 0 | - - - - - - - - - - - - HAM | |
| 80000 | 4 | Inflammatory disorders | |
| 80100 | 1 | - - - - - - Behcet's disease | |
| 80200 | 2 | - - - - - - Sarcoidosis | |
| 80300 | 4 | - - - - - - Paraneoplastic encephalomyelopathy | |
| 90000 | 18 | Prion disease | |
| 90100 | 5 | - - - - - - sporadic Prion disease | |
| 90200 | 1 | - - - - - - inherited Prion disease | |
| 90300 | 0 | - - - - - - acquired Prion disease | |
| 100000 | 9 | Vascular disorders | |
| 100100 | 289 | - - - - - - Infarction | |
| 100200 | 63 | - - - - - - Hemorrhage | |
| 100300 | 0 | - - - - - - Amyloid angiopathy | |
| 100400 | 2 | - - - - - - Binswanger disease | Binswanger |
| 100500 | 15 | - - - - - - hypoxic ischemic encephalopathy | |
| 110000 | 4 | Intoxication | |
| 110100 | 0 | - - - - - - CO | |
| 110200 | 0 | - - - - - - Mechylmercury / Minanamata disease | |
| 110300 | 0 | - - - - - - SMON | |
| 110400 | 1 | - - - - - - Alcohol | |
| 110500 | 4 | - - - - - - Hepatic | |
| 120000 | 0 | Inborn errors of metabolism | |
| 120100 | 0 | - - - - - - Lysosomal disorders | |
| 120200 | 0 | - - - - - - Peroxisomal disorders | |
| 120201 | 0 | - - - - - - - - - - - - X-linked adrenoleukodystrophy | |
| 120300 | 6 | - - - - - - Mitocondrial disorders | |
| 120400 | 0 | - - - - - - Cockayne syndrome | |
| 120500 | 1 | - - - - - - Xeroderma pigmentosum | |
| 120600 | 1 | - - - - - - Alexander's disease | |
| 130000 | 3 | Congenital malformations | |
| 130100 | 0 | - - - - - - Anencephaly | |
| 130200 | 1 | - - - - - - Hydrocephalus | |
| 130300 | 0 | - - - - - - Lissencephaly | |
| 130400 | 0 | - - - - - - Holoprocencephaly | |
| 130500 | 0 | - - - - - - Tuberous sclerosis | |
| 130600 | 0 | - - - - - - Trisomy | |
| 140000 | 7 | Myopathy | |
| 140100 | 1 | - - - - - - Myasthenia gravis | |
| 140200 | 7 | - - - - - - Muscular dystrophy | |
| 140201 | 5 | - - - - - - - - - - - - Duchenne muscular dystrophy | |
| 140202 | 0 | - - - - - - - - - - - - Fukuyama congenital muscular dystrophy | |
| 140203 | 27 | - - - - - - - - - - - - Myotonic dystrophy | |
| 140300 | 3 | - - - - - - Myositis | |
| 150000 | 3 | Peripheral neuropathy | |
| 150100 | 1 | - - - - - - Guillan-Barre syndrome | |
| 150200 | 1 | - - - - - - CIDP | |
| 150300 | 1 | - - - - - - Hereditary neuropathy | |
| 160000 | 45 | Tumors | |
| 160100 | 4 | - - - - - - Gliomas | |
| 160101 | 0 | - - - - - - - - - - - - Astrocytic and oligodendroglial tumors | |
| 160102 | 0 | - - - - - - - - - - - - Ependymal tumors | |
| 160200 | 0 | - - - - - - Neuronal and mixed neuronal-glial tumors | |
| 160300 | 0 | - - - - - - Embryonal tumors | |
| 160400 | 1 | - - - - - - Schwannomas | |
| 160500 | 14 | - - - - - - Meningiomas | |
| 160600 | 11 | - - - - - - Lymphomas | |
| 160700 | 0 | - - - - - - Germ cell tumors | |
| 160800 | 0 | - - - - - - Tumors of the sellar region | |
| 160801 | 0 | - - - - - - - - - - - - Pituitary adenoma | |
| 170000 | 6 | Epilepsy | |
| 170100 | 0 | - - - - - - Myoclonic epilepsy | |
| 170200 | 0 | - - - - - - Mesial temporal sclerosis / Hippocampal sclerosis | |
| 170300 | 0 | - - - - - - Neocortical epilepsies | |
| 180000 | 4 | Trauma | |
| 190000 | 0 | Perinatal disorders | |
| 190100 | 0 | - - - - - - CP | |