- Subacute Encephalopathies (Rapidly Progressive Dementias)
- Non-vasculitic Autoimmune Inflammatory Meningoencephalitis (NAIM)
- Glucose Transporter Type I Deficiency Syndrome GLUT1 DS
- Niemann-Pick Disease
- Porphyria
- Cerebrotendinous Xanthomatosis
- Refsum Disease
- Zellweger Syndrome
- Megalencephalic Leukodystrophy with Subcortical Cysts
- Vanishing White Matter disease VWM
- Pelizaeus-Merzbacher-Like Disease
- Pelizaeus Merzbacher Disease PMD
- Sudanophilic Leukodystrophy
- Canavan Disease
- Alexander Disease
- Adrenoleukodystrophy and Adrenomyeloneuropathy
- Krabbe Disease (Globoid Cell Leukodystrophy)
- Metachromatic Leukodystrophy MLD
- Leukodystrophy
- Necrotizing Autoimmune Myopathy NAM
- Bilateral Striatal Necrosis
- Leigh’s disease (Subacute necrotizing encephalomyelopathy)
- Mitochondrial Neurogastrointestinal Encephalomyopathy MNGIE
- Alper Syndrome
- Kearns-Sayre Syndrome KSS
- Mitochondrial Disorders
- Lipid Storage diseases
- Myoadenylate Deaminase Deficiency MAD deficiency
- Sporadic Late Onset Nemaline Myopathy SLONM
- Condrodystrophic Myotonia
- Paramyotonia Congenita
- Non-Dystrophic Myotonias
- Myotonia Congenita
- Proximal Myotonic Myopathy
- Myotonic Dystrophy DM1
- Congenital Muscular Dystrophies CMD
- Oculopharyngeal Dystrophy OPMD
- Fascioscapulohumeral Myopathy FSH
- Emery-Dreifuss Muscular Dystrophy
- Becker Muscular Dystrophy, BMD
- Glycogenoses (glycogen storage diseases)
- Congenital Myopathies
- Limb Girdle Muscular Dystrophies LGMDs
- Duchenne Muscular Dystrophy, DMD
- Malignant Hyperthermia Syndrome
- Hyperkalemic Periodic Paralysis
- Hypokalemic Periodic Paralysis
- Dyskalemic Myopathy
- Statin Myopathy
- Drug Induced Myopathies
- Critical Care Myopathy
- Corticosteroid Myopathy
- Eosinophilic Myositis and Eosinophilic Fasciitis
- Macrophagic Myofasciitis MMF
- Nodular Focal Myositis
- Polymyalgia Rheumatica
- Inclusion Body Myositis
- Parasitic Myositis
- Bacterial Myositis
- Viral Myositis
- Myoglobinuria
- Rhabdomyolysis
- Denervation Atrophy
- Idiopathic Cramps
- Paroxysmal Extreme Pain Disorder PEPD
- Morvan's fibrillary chorea, Morvan's syndrome, neuromyotonia NMT, and Isaac syndrome
- Pure autonomic failure (PAF)
- Autoimmune Autonomic Ganglionopathy AAG
- Chronic Idiopathic Axonal Polyneuropathy CIAP
- Idiopathic Sensory Ganglionopathy
- Hereditary sensory neuropathy HSN (Hereditary sensory autonomic polyneuropathy HSAN)
- Fabry Disease: alpha-galactosidase A deficiency
- Tangier disease: Familial alpha-lipoprotein deficiency
- Sjogren Syndrome Neuropathy
- Coeliac Disease Neuropathy
- Idiopathic Sensory Perineuritis
- Migrant sensory neuritis (Wartenberg Syndrome)
- Nonhereditary Amyloid Neuropathy
- Mycobacterium leprae Neuropathy
- HIV Neuropathy
- Heavy Metal Neuropathy and Solvent Neuropathy
- Alcohol Neuropathy
- Chronic Renal Failure Neuropathy
- Hypophosphatemia Neuropathy
- Nutritional Deficiency Neuropathy
- Charcot-Marie-Tooth disease CMT
- Acromegaly Neuropathy
- Cranial Neuropathies
- Diabetic Neuropathy
- Paraneoplastic Sensory Neuropathy
- Paraneoplastic Vasculitic Neuropathy PVN
- Nonsystemic vasculitic neuropathy NSVN
- Systemic Vasculitic Neuropathy
- Anti-sulfatide Neuropathy
- Anti-GALOP syndrome: Gait ataxia, autoantibody, late onset polyneuropathy
- Lymphoma Associated Neuropathy
- Anti-MAG syndrome
- POEMS syndrome: Polyneuropathy Organomegally Endocrinopathy M protein and Skin changes
- Polyeuropathy Associated with Paraproteinemia
- Multifocal Acquired Demyelinating Sensory And Motor neuropathy MADSAM
- Subacute Inflammatory Demyelinating Polyneuropathy
- Radiation Induced Radiculopathy
- Critical Care Neuropathy CIP
- Idiopathic Lumbosacral Plexitis
- Radiation Induced Plexopathies (Radiation Plexopathy)
- Heredofamilial Brachial Plexopathy
- Carcinomatous Plexopathy
- Acute Brachial Plexus Neuritis
- Neurogenic Thoracic Outlet Syndrome
- Autonomic Neuropathy
- Radiculopathy
- Polyradiculopathy
- Brachial Plexopathy
- Congenital Myasthenic Syndromes
- Neonatal Myasthenia
- Clostridium tetani (tetanus)
- Clostridium botulinum neurotoxin (Botulism)
- Lambert Eaton Myasthenic Syndrome LEMS
- Mononeuropathy Multiplex
- Neuromuscular Junction Disorders NMJ
- Small Fibre Sensory Neuropathy SFSN
- Polyneuropathy
- Electrical injury to anterior horn cells
- Mononeuropathy
- Tremor
- Spinal and bulbar muscular atrophy, Kennedy disease
- Primary Lateral Sclerosis
- Poliomyelitis
- Lissencephaly
- Hydranencephaly
- Spinal Muscular Atrophy
- Cryoglobulinemia, Neurological Manifestations
- Behcet's Syndrome
- Giant Cell Arteritis
- Takayasu’s Disease
- Familial amyloid polyneuropathy FAP
- Neurosarcoidosis, Sarcoid disease Neurological Manifestations
- Febrile Seizures
- General Learning Disability
- Tuberous Sclerosis
- Encephalofacial Angiomatosis, Sturge-Weber disease
- Familial Hyperekplexia
- Benign Paroxysmal Torticollis
- Cyclic vomiting syndrome
- Tongue-Neck Syndrome
- Skull Base Syndromes
- Isolated Facial palsy, CN VII
- Mental Neuropathy
- Parinaud Syndrome
- Acquired Oculomotor Apraxia
- Superior Orbital Fissure Syndrome
- Cavernous Sinus Syndrome
- Tolosa Hunt Syndrome
- Internuclear Ophthalmoplegia (INO)
- Abducens (cranial nerve VI palsy)
- Trochlear Nerve Palsy (Cranial IV palsy)
- Oculomotor Palsy (cranial nerve III palsy)
- Horner Syndrome
- Cancer-associated retinopathy (CAR)
- Nystagmus
- Ataxia
- Chorea, in general
- Myoclonus
- Hemiballismus
- Dystonia, in general
- Leukoencephalopathy (white matter disease)
- Charles Bonnet Syndrome
- Klüver-Bucy syndrome
- Alien Limb Syndrome
- Balint’s Syndrome
- Mild Cognitive Impairment (MCI)
- Dementia
- Catatonia
- Raised Intracranial Pressure, raised ICP
- Cerebral Edema
- Chiari Malformation
- JC virus Granule Cell Neuronopathy (JCV GCN)
- Bickerstaff Brainstem Encephalitis (BBE)
- Osmotic Demyelination Syndrome
- Organic-Solvent Related Acute Leukoencephalopathy
- Heroin related Acute leukoencephalopathy “chasing the dragon"
- Hashimoto Encephalopathy
- Progressive Multifocal Leukoencephalopathy (PML)
- Disseminated Necrotizing Leukoencephalopathy (DNL)
- Acute Disseminated Encephalomyelitis (ADEM)
- Empty Sella Syndrome
- Biotin-Responsive Encephalopathy
- Wernicke Encephalopathy
- Normal Pressure Hydrocephalus
- Frontotemporal Dementia (FTD)
- Vascular Parkinsonism
- Vascular Dementia
- Transient Global Amnesia
- Kuru
- Gerstmann–Sträussler–Scheinker Syndrome:
- Fatal Familial Insomia
- Variant Creudtzfedt-Jakob Disease (vCJD)
- Sporadic Creutzfeldt-Jakob Disease (sCJD)
- Fungal Intracranial Abscess
- Spinal Cord Abscess
- Epidural Abscess (intracranial or spinal)
- Brain Abscess
- Intracranial Empyema
- Subacute Sclerosing Panencephalitis (SSPE)
- HIV Associated Neurocognitive Disorders (HAND)
- Nonparaneoplastic Autoimmune Limibic Encephalitis
- Paraneoplastic Encephalomyelitis, Paraneoplastic Encephalitis
- Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS)
- Idiopathic Hypertrophic Cranial Pachymeningitis
- Optic Neuritis
- Neuromyelitis Optica
- Lumbar spinal stenosis
- Spondylolisthesis and Spondylolysis
- Cervical Spondylosis
- Subacute Combined Degeneration of the Spinal Cord
- Syringomyelia
- Radiation Induced Spinal Cord Hemorrhage
- Radiation Myelopathy
- Schistosomal Myeloradiculopathy
- HTLV-1 Myelitis
- Viral Myelitis
- Idiopathic Acute Transverse Myelitis
- Spinal Cord Infarction
- Spinal Cord compression (compression myelopathy)
- Postural orthostatic tachycardia syndrome (POTS)
- Carotid Sinus Syncope
- Simple Faints
- Orthostatic Hypotension
- Subclavian Steal Syndrome
- Chilhood Epilepsy Syndromes
- Autosomal dominant partial epilepsy with auditory features (ADTLE)
- Generalised epilepsy with febrile seizures plus (GEFS+)
- Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (ADNFLE)
- Benign Familial Neonatal Seizures
- Myoclonic Astatic Epilepsy of Childhood
- Severe Myoclonic Epilepsy of Infancy
- Focal epilepsy (cryptogenic, symptomatic)
- Idiopathic generalized epilepsy with Generalized tonic-clonic seizures only
- Juvenile Myoclonic Epilepsy (JME)
- Benign epilepsy with centrotemporal spikes (BECTS)
- Lennox-Gestuat Syndrome
- Aicardi Syndrome
- West Syndrome
- Juvenile Absence Epilepsy
- Progressive Myoclonic Epilepsy (PME)
- Neuronal Ceroid Lipofuscinosis
- GM2 Gangliosidosis, Hexosaminidase Deficiency
- Gaucher Disease
- Myoclonic Epilepsy and Ragged Red Fibres (MERRF)
- Juvenile Neuroaxonal Atrophy
- Sialidosis
- Lafora Disease
- Unverricht-Lundborg Disease
- Nitromethane Encephalopathy
- Alcohol Withdrawal
- Neurocysticercosis
- Rasmussen Encephalitis
- Transient Epileptic Amnesia
- Gastaut-Geschwind Syndrome
- Heterotopia
- Mesotemporal Sclerosis
- Status Epilepticus
- Congenital Central Hypoventilation Syndrome
- Obstructive Sleep Apnea
- Somnambulism
- REM Sleep Behaviour Disorder
- Nightmares
- Night Terrors
- Periodic Limb Movements of Sleep
- Advanced Sleep Phase Syndrome
- Restless Leg Syndrome
- Kleine-Levin Syndrome
- Narcolepsy
- Delayed Sleep Phase Syndrome
- Insomnia
- Perineural Cyst
- Enterogenous Cyst
- Dermoid Cyst
- Epidermoid Cyst
- Arachnoid Cyst
- Meningeal cyst
- Retinoblastoma
- Paraganglioma
- Chordoma
- Intraneural Perineuroma
- Neurofibromatosis (NF)
- Neurofibroma
- Schwannoma
- Meningioma
- Colloid Cyst:
- Secondary CNS Lymphoma
- Lymphomatoid granulomatosis (LG)
- Intravascular B cell Lymphoma
- Primary CNS lymphoma (PCNSL)
- Hypothalamic Hamartoma
- Pineoblastoma
- Pineocytoma
- Germinoma
- Rathke Cleft Cyst
- Craniopharyngioma
- Pituitary adenoma
- Atypical teratoid rhabdoid tumor (ATRT)
- Neuroblastoma, Olfactory
- Primitive Neuroectodermal Tumor (PNET)
- Medulloblastoma
- Choroid Plexus Papilloma
- Central Neurocytoma
- Hemangioblastoma
- Desmoplastic infantile ganglioglioma (DIG) and desmpolastic infantile astrocytoma
- Dysembryoplastic neuroepithelial tumor DNET
- Gangliocytoma and Ganglioglioma
- Astroblastoma
- Ependymoma
- Oligodendroglioma
- Gliomatosis Cerebri
- Brain Tumor
- Glioblastoma
- Anaplastic Astrocytoma
- Diffuse Astrocytoma
- Pleomorphic Xanthoastrocytoma PXA
- Subependymal Giant Cell Astrocytoma SEGA
- Pilocytic Astrocytoma
- Fahr disease
- Neuroacanthocytosis
- Dentatorubropallidoluysian atrophy DRPLA
- Hypoxanthine-guanine phosphoribosyltransferase HPRT deficiency
- Hereditary ferritinopathy and neurodegeneration with brain iron accumulation type 2 NIBA2
- Pantathenate kinase deficiency Associated Neurodegeneration
- Chronic Carbon Monoxide CO poisoning
- Opsoclonus Myoclonus
- Hemifacial Spasm
- Stiff Person Syndrome
- Metoclopramide induced Akathesia
- Tardive Dyskinesia
- Genetic Dystonia
- Paroxysmal Dyskinesia
- Meige Syndrome
- Generalised Dystonia or Segmental Dystonia
- Focal Dystonia
- Tourette’s syndrome
- Periodic Alternating Nystagmus PAN
- Anti-GAD antibodiy associated progressive cerebellar ataxia
- Paraneoplastic Cerebellar Degeneration
- Fragile X Tremor Ataxia syndrome
- Episodic Ataxia type 2
- Episodic Ataxia type 1
- Spinocerebellar Ataxias
- Ataxia with Vitamin E Deficiency
- Friedreich’s Ataxia
- Gluten Ataxia
- Acute Post-Infectious Cerebellitis
- Progressive Ataxia and Palatal Tremor
- Oculopalatal Tremor
- Rubral Tremor
- Cerebellar Tremor
- Orthostatic Tremor
- Wilson's disease
- Neurofilament inclusion body disease NIBD
- Argyrophilic grain disease AGD
- Corticobasal Degeneration
- Progressive Supranuclear Palsy
- Multiple System Atrophy
- Post-Encephalitic Parkinsonism
- Serotonin Syndrome
- Neuroleptic Malignant Syndrome
- Burning mouth syndrome
- Complex Regional Pain Syndromes CRPS
- Persistent Idiopathic Facial Pain
- Neck-tongue syndrome
- Temoporomandibular joint TMJ syndrome
- Post-Herpetic Neuralgia
- Glossopharyngeal Neuralgia
- Trigeminal Neuralgia
- Idiopathic Stabbing Headache
- Medication Overuse Headache
- New Daily Persistent Headache
- Chronic Daily Headache
- Hypnic Headache
- Hemicrania Continua
- Short-lasting Unilateral Neuralgiform headache attacks with Conjunctival injection and Tearing (SUNCT)
- Paroxysmal Hemicrania
- Cluster Headache
- Ophthalmoplegic "Migraine"
- Familial Hemiplegic Migraine
- Slit Ventricle Syndrome
- Spontaneous Intracranial Hypotension
- Idiopathic Intracranial Hypertension
- Post Lumbar Puncture Headache
- Primary Thunderclap Headache
- Primary headache associated with sexual activity
- Cerebral Palsy
- Dolichoectasia of intracranial arteries
- Vertebral Artery Stenosis, Extracranial
- Vertebral Artery Stump Syndrome
- Carotid Stump Syndrome
- Ischemic Stroke with Patent Foramen Ovale
- Varicella Zoster Virus VZV vasculopathy
- Spinal epidural venous engorgement of pregnancy
- Bell's Palsy
- Traumatic nerve root avulsion
- Diffuse Axonal Injury
- Cerebral Contusion
- Subdural Hematoma
- Epidural Hematoma
- Concussion
- Traumatic Brain Injury
- Subcortical Arteriosclerosis Encephalopathy
- Primary Angiitis of the Central Nervous System
- Reversible Cerebral Vasoconstriction Syndrome
- Cervical Artery Dissection
- Radiation Vasculopathy
- Fibromuscular Dysplasia
- Intracranial Atherosclerotic Disease
- Carotid Artery Stenosis, Extracranial
- Cardioembolic Stroke
- Small Vessel Disease
- Transient Ischemic Attack
- Cerebral Amyloid Angiopathy
- Cavernous Malformation
- Spinal Vascular Lesions
- Capillary telangiectasia
- Sinus pericranii
- Developmental Venous Anomaly
- Vein of Galen malformation
- Vertebral arteriovenous fistula
- Carotid Cavernous Fistula
- Dural Arteriovenous Fistula, Cranial
- Arteriovenous Malformations
- Infundibulum
- Cerebral Pseudoaneurysms
- Blister Like Pseudoaneurysm
- Cerebral Aneurysms, Fusiform
- Cerebral Aneurysms, Saccular
- Superficial Siderosis
- Perimesenchphalic Subarachnoid Hemorrhage
- Post-Anoxic Myoclonus
- Anoxic Brain Injury
- Posterior Reversible Leukoencephalopathy Syndrome PRES
- Degos disease
- Eales Disease
- Susac’s syndrome
- Alagille syndrome
- Cerebral Autosomal Dominant Arteriopathy and Subacute Infarcts with Leukoencephalopathy
- Postpartum Cerebral Angiopathy
- Cerebral Venous Sinus Thrombosis
- Moyamoya disease
- Posterior Cortical Atrophy
- Polymyositis
- Dermatomyositis
- Huntington Disease
- Diffuse Lewy Body Disease
- Essential Tremor
- Chronic Inflammatory Demyelinating Polyradiculopathy
- Epilepsy
- Lumbosacral Plexopathy
- Subarachnoid Hemorrhage
- Intracerebral Hemorrhage
- Hemorrhagic Stroke
- Ischemic Stroke
- Listeria Rhombencephalitis
- Viral Encephalitis
- Tension-Type Headache
- Encephalitis
- Fungal Meningitis
- Tuberculous Meningitis
- Viral Meningitis
- Bacterial Meningitis
- Meningitis
- Amyotrophic Lateral Sclerosis
- Parkinson's Disease
- Myasthenia Gravis
- Alzheimer Disease
- Guillain-Barre Syndrome
- Tick Paralysis
- Diphtheria Polyneuritis
- Multifocal Motor Neuropathy
- Neurolgical Diseases list
- Nerve diseases
- Myopathy (Muscle diseases)
- Migraine
- Multiple Sclerosis
- Myelopathy