| Cardiovascular
|
Arteriosclerosis, Circulation disorders in area of brain stem, Morgagni’s Syndrome
|
| Chemical / poisoning
|
2,4,6-Trichlorophenol, Acrylamide, Aftershave, Amitraz, Aniline, Antifreeze, Apple seed poisoning, Arizona Bark Scorpion poisoning, Benzene, Blue-ringed octopus poisoning, Buckeye poisoning, Carbon monoxide poisoning, Death Camas poisoning, English Ivy poisoning, Ethotoin, Galantamine hydrobromide, Gasoline, Lantana poisoning, Lead, Mayapple poisoning, Mercury, Mescal poisoning, Minamata disease, Mistletoe poisoning, Thallium poisoning, Tolterodine toxicity, Toxic mushrooms — Anticholinergic, Toxic mushrooms — Monomethylhydrazine, Toxic mushrooms — Psychedelic, Varnish makers’ and painters’ Naptha, Xylene
|
| Dermatologic
|
Erythrokeratodermia with ataxia, Tranebjaerg-Svejgaard syndrome, DeSanctis-Cacchione syndrome, Xeroderma pigmentosum
|
| Drug Side Effect
|
Agalsidase beta, Alprazolam, Amobarbital sodium, Artemether and lumefantrin, Atroine, Amiodarone, Barbituates, Benzodiazepines, Carbamazepine, Chlordiazepoxide, Cidofovir, Cytarabine, Eslicarbazepine acetate, Estazolam, Ethosuximide, Flurazepam hydrochloride, Flurbiprofen, Flucytosine, Gabapentin, Hydroxychloroquine, Lacosamide, Lamotrigine, Levetiracetam, Loxapine, lomustine, Metronidazole, Morphine, Meprobamate, Nabilone, Nelarabine, Olanzapine,oxazepam Oxcarbazepine, Perampanel, Pergolide, Perphenazine, Phenytoin, Polymyxin B, Primidone, Rufinamide, Secobarbital sodium, Sertraline, Spironolactone, Topiramate
|
| Ear Nose Throat
|
Acoustic neurinoma, Benign Paroxysmal Positional Vertigo, Reardon-Wilson-Cavanagh syndrome, Richards-Rundle syndrome, Susac syndrome, Treft-Sanborn-Carey syndrome
|
| Endocrine
|
Adult-onset adreno leukodystrophy, Diabetic neuropathy, Functioning pancreatic endocrine tumor, Furukawa-Takagi-Nakao syndrome, Hypogonadism, Hypothyroidism, Insulinoma, Metastatic insulinoma, Morgagni’s Syndrome
|
| Environmental
|
Acute altitude sickness
|
| Gastroenterologic
|
Bassen-Kornzweig syndrome, Celiac disease, Cirrhosis, Dykes-Markes-Harper syndrome, Hepatocerebral degeneration, Wilson’s Disease
|
| Genetic
|
Alpers Syndrome, Angleman syndrome, Bangstad syndrome, Bassen-Kornzweig syndrome, Bhaskar-Jagannathan syndrome, Cerebellar ataxia, Cockayne syndrome, Dravet syndrome, Familial isolated deficiency of vitamin E, Familial periodic ataxia, Feline spongiform encephalopathy, Friedreich’s ataxia, Griscelli disease, Hallervorden-Spatz disease, Hereditary spastic paraparesis, Krabbe leukodystrophy, Richards-Rundle syndrome, Roussy-Levy syndrome, Rubinstein-Taybi syndrome, Sialidosis type 1 and 3, Tranebjaerg-Svejgaard syndrome, Xeroderma pigmentosum, X-linked sideroblastic anaemia
|
| Hematologic
|
Acanthocytosis, Aceruloplasminemia, Macrocytic anemia, Pernicious anemia, Revesz Debuse syndrome, X-linked sideroblastic anaemia
|
| Iatrogenic
|
No underlying causes
|
| Infectious Disease
|
Brain abscess, Cerebellar abscess, Chickenpox, Diphtheria, Encephalitis, HIV infection, Measles, Quaternary syphilis, Ramsay-Hunt syndrome, Smallpox, Tabes dorsalis
|
| Musculoskeletal / Ortho
|
Dinno-Shearer-Weisskopf syndrome, Furukawa-Takagi-Nakao syndrome, Myopathy
|
| Neurologic
|
Acute Disseminated Encephalomyelitis, Alexander Syndrome, Alpers Syndrome, Arachnoid Cysts, Arnold-Chiari Malformation, ARTS syndrome, Ataxia deafness reardon type, Ataxia tapetoretinal degeneration, Ataxia telangiectasia / Louis-Bar syndrome, Ataxia-oculomotor apraxia syndrome, Basal ganglia calcification, Basilar artery migraine, Vertebro-basilar artery ischemia, Brain abscess, Brain cancer, Brain cyst, Brain injury, Brainstem or cortical lesions, Central nervous system lymphoma, primary, Cerebellar abscess, Cerebellar ataxia, Cerebellar cortex atrophy, Cerebellar degeneration, Cerebellar haemorrhage, Cerebellar heredoataxia, Cerebellar hypoplasia, Cerebellar infarct, Cerebellar mass, Cerebral Amyloid Angiopathy, Familial, Cerebral hemorrhage, Cerebral infarction, Cerebral palsy, Cerebrorenodigital syndrome, Cerebrovascular accident, Ceroid lipofuscinosis, Cervical myelopathy, Chorea familial benign, Chronic progressive traumatic encephalopathy, Cockayne syndrome, Combarros Calleja Leno syndrome, Corneal cerebellar syndrome, Creutzfeldt-Jakob disease, Cutler-Bass-Romshe syndrome, Dandy-Walker Syndrome, Dementia pugilis, Demyelinating disorder, DeSanctis-Cacchione syndrome, Dinno-Shearer-Weisskopf syndrome, Dravet syndrome, Dykes-Markes-Harper syndrome, Dysequilibrium syndrome, Encephalitis, Encephalocele frontal, Epiphyseal tumor, Episodic ataxia, Erythrokeratodermia with ataxia, Feline spongiform encephalopathy, Fisher’s Syndrome, Friedreich’s ataxia, Frontal lobe lesion, GALOP Syndrome (gait disorder, autoantibodies, late age onset, polyneuropathy), Glioma, Granulomatous Angiitis of the central nervous system, Guillain-Barré syndrome, Hallervorden-Spatz disease, Heidenhain syndrome, Hepatocerebral degeneration, Hydrocephalus, Infantile polymyoclonus, Inherited neuropathies, Joubert syndrome, Juvenile pilocytic astrocytoma, Kearns-Sayre Syndrome, Kuru, Lhermitte-McAlpine syndrome, Machado-Joseph Disease, Macrogyria, pseudobulbar palsy and mental retardation, Mann Syndrome, Marinesco-Sjogren-like syndrome (MSLS), Marinescu-Garland Syndrome, Medulloblastoma, Meinecke syndrome, Meningoencephalocele, Mental retardation progressive spasticity, X-linked, Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, Metachromatic Leukodystrophy, Miller Fisher Syndrome, Mitochondrial encephalomyopathy, Mononeuropathy/radiculopathy affecting the lower extremities, Multiple sclerosis, Myelopathy, Myoclonus, Neuronal intranuclear hyaline inclusion disease, Normal pressure hydrocephalus, Olivopontocerebellar atrophy, Opsoclonus myoclonus syndrome, Parietal lobe lesion, Parkinson’s disease, Partington X-linked mental retardation syndrome, Pelizaeus-Merzbacher disease, Peripheral neuropathy, Polyneuritis, Polyneuropathy, Post-infective polyradiculopathy, Posterior column ataxia with retinitis pigmentosa, Posterior fossa tumor, Progressive Multifocal Leukoencephalopathy, Reardon-Wilson-Cavanagh syndrome, Rett syndrome, Rhombencephalosynapsis, Roussy-Levy syndrome, Schroer-Hammer-Mauldin syndrome, Segawa syndrome, autosomal recessive, Shy-Drager syndrome, Spastic paraplegia, Spinal cord compression (and pressure on dorsal nerve roots), Spinal cord tumor, Spinocerebellar ataxia, Spinocerebellar degenerescence, book type, Stroke, Susac syndrome, Tabes dorsalis, Telencephalic leukoencephalopathy, Thalamic syndrome, Thoracic dysplasia — hydrocephalus syndrome, Tranebjaerg-Svejgaard syndrome, Transient ischemic attack (TIA), Transverse myelitis, Vascular dementia, Vertebral Artery Dissection, Vertebrobasilar dolichoectasia, Vertigo, benign paroxysmal, Westphal’s Disease, Wilson’s Disease
|
| Nutritional / Metabolic
|
Abetalipoproteinemia, Alpha-ketoglutarate dehydrogenase deficiency, Aminoaciduria, Argininosuccinase lyase deficiency – late onset, Arginosuccinate synthetase deficiency, Ataxia with Vitamin E Deficiency, Biotinidase deficiency, Ceruloplasmin deficiency, Cholestanol storage disease, Coenzyme Q 10 (CoQ10), deficiency, Complex 2 mitochondrial respiratory chain deficiency, Congenital Disorders of Glycosylation, Cystinuria — lysinuria, Fabry’s Disease, Gangliosidosis GM1 type 3, Gaucher disease type 2, Glutathione synthase deficiency, Glycine encephalopathy, atypical mild form, GM2-gangliosidoses, Hartnup Disease , Hexosaminidase deficiency, Homozygous hypobetalipoproteinemia, Hydroxyacyl-coa dehydrogenase, type 2, deficiency, Infantile sialic acid storage disorder, Lactic acidosis congenital infantile, Lipoamide dehydrogenase deficiency, Maple syrup urine disease, Mevalonic aciduria, Mitochondrial cytopathy, Niemann-Pick disease, Pellagra-like syndrome, Phosphoribosylpyrophosphate synthetase superactivity, Purine nucleoside phosphorylase deficiency, Pyruvate dehydrogenase deficiency, Refsum Disease, Selective vitamin E deficiency, Sialidosis type 1 and 3, SSADH deficiency (succinic semialdehyde dehydrogenase deficiency), Thiamine deficiency, Triglyceride storage disease with impaired long-chain fatty acid oxidation, Vitamin B12 deficieny, Wernicke-Korsakoff psychosis, Zinc deficiency
|
| Obstetric/Gynecologic
|
No underlying causes
|
| Oncologic
|
Acoustic neurinoma, Brain cancer, Bronchogenic carcinoma, Central nervous system lymphoma, primary, Epiphyseal tumor, Functioning pancreatic endocrine tumor, Glioma, Insulinoma, Juvenile pilocytic astrocytoma, Medulloblastoma, Metastatic insulinoma, Paraneoplastic syndromes, Posterior fossa tumor, Spinal cord tumor
|
| Opthalmologic
|
Combarros Calleja Leno syndrome, Corneal cerebellar syndrome, Fisher’s Syndrome, Marinesco-Sjogren-like syndrome (MSLS), Posterior column ataxia with retinitis pigmentosa, Refsum Disease, Revesz Debuse syndrome, Schroer-Hammer-Mauldin syndrome, Susac syndrome, Treft-Sanborn-Carey syndrome
|
| Overdose / Toxicity
|
Lithium toxicity, Phenytoin toxicity
|
| Psychiatric
|
Hysteria
|
| Pulmonary
|
Bronchogenic carcinoma, Prolonged anoxia
|
| Renal / Electrolyte
|
Cerebrorenodigital syndrome, Cutler-Bass-Romshe syndrome
|
| Rheum / Immune / Allergy
|
ARTS syndrome, Griscelli disease, Fisher’s Syndrome
|
| Sexual
|
No underlying causes
|
| Trauma
|
Brainstem or cortical lesions, Frontal lobelesion, Mann Syndrome, Parietal lobelesion, Head trauma
|
| Urologic
|
No underlying causes
|
| Miscellaneous
|
Alcohol intoxication, Amyloidosis, oculoleptomeningeal, Arteriosclerosis, Bonnemann-Meinecke-Reich syndrome, Chitayat-Moore-Del Bigio syndrome, Hemangioblastoma, Hyperammonemia, sporadic ataxia, Tick paralysis, Transthyretin amyloidosis
|
