Condition library · 293 conditions
Neurology conditions
Conditions of the brain, spinal cord, nerves and muscles.
Doctors for these conditions are listed as neurologists.
All neurology conditions
A
- Aceruloplasminemia
- Action myoclonus–renal failure syndrome
- Acute Flaccid Myelitis
- Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
- Acute necrotizing encephalopathy type 1
- Adenylosuccinate lyase deficiency
- ADNP syndrome
- Adult-onset autosomal recessive cerebellar ataxia
- Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
- Aicardi-Goutières syndrome
- Alexander disease
- Allan-Herndon-Dudley syndrome
- Alternating hemiplegia of childhood
- Alzheimer's Disease
- Aminoacylase 1 deficiency
- Amyotrophic Lateral Sclerosis
- Andermann syndrome
- Andersen-Tawil syndrome
- Anencephaly
- Angelman syndrome
- Anoctamin-5-related limb-girdle muscular dystrophy R12
- Aphasia
- Asparagine synthetase deficiency
- Ataxia neuropathy spectrum
- Ataxia Telangiectasia
- Ataxia with oculomotor apraxia
- Ataxia with vitamin E deficiency
- Ataxia-pancytopenia syndrome
- Atypical Rett syndrome
- Autosomal dominant cerebellar ataxia, deafness, and narcolepsy
- Autosomal dominant Charcot-Marie-Tooth disease type 2A2
- Autosomal dominant Charcot-Marie-Tooth disease type 2Z
- Autosomal dominant epilepsy with auditory features
- Autosomal dominant sleep-related hypermotor epilepsy
- Autosomal dominant spastic paraplegia type 10
- Autosomal recessive axonal neuropathy with neuromyotonia
- Autosomal recessive cerebellar ataxia type 1
- Autosomal recessive cerebellar ataxia with late-onset spasticity
- Autosomal recessive cerebelloparenchymal disorder type 3
- Autosomal recessive myogenic arthrogryposis multiplex congenita
- Autosomal recessive spastic ataxia of Charlevoix-Saguenay
- Autosomal recessive spastic paraplegia type 35
- Autosomal recessive spastic paraplegia type 46
- Autosomal recessive spastic paraplegia type 55
- Autosomal recessive spastic paraplegia type 77
- Autosomal recessive spastic paraplegia type 78
- Autosomal spastic paraplegia type 58
B
C
- Canavan disease
- Cap myopathy
- CDKL5 deficiency disorder
- Central core disease
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Cerebral folate transport deficiency
- Cerebral Palsy
- Charcot-Marie-Tooth disease type 1E
- Charcot-Marie-Tooth disease type 1F
- Charcot-Marie-Tooth disease type 4A
- Charcot-Marie-Tooth disease type 4B2
- Charcot-Marie-Tooth disease type 4C
- CHD2 myoclonic encephalopathy
- Childhood absence epilepsy
- Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
- CHMP2B-related frontotemporal dementia
- Chorea-acanthocytosis
- Chronic Pain
- CLCN2-related leukoencephalopathy
- CLN1 disease
- CLN10 disease
- CLN11 disease
- CLN2 disease
- CLN3 disease
- CLN4 disease
- CLN5 disease
- CLN6 disease
- CLN7 disease
- CLN8 disease
- Coats plus syndrome
- Cold-induced sweating syndrome
- Coma
- Complex Regional Pain Syndrome
- Concussion
- Congenital central hypoventilation syndrome
- Congenital insensitivity to pain with anhidrosis
- Congenital muscular dystrophy with intellectual disability
- Congenital muscular dystrophy without intellectual disability
- Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome
- Congenital myasthenic syndromes
- Constitutional mismatch repair deficiency syndrome
- Creutzfeldt-Jakob Disease
D
- Dementia
- Dementia with Lewy bodies
- Dentatorubral-pallidoluysian atrophy
- Developmental and epileptic encephalopathy 1
- Distal hereditary motor neuropathy, type II
- Distal hereditary motor neuropathy, type V
- Dopa-responsive dystonia
- Dopamine transporter deficiency syndrome
- Duchenne and Becker muscular dystrophy
- Dysequilibrium syndrome
- Dystonia
- Dystonia 16
- Dystonia 6
- Dystonia-parkinsonism-hypermanganesemia syndrome
E
F
- Facioscapulohumeral muscular dystrophy
- Familial dysautonomia
- Familial encephalopathy with neuroserpin inclusion bodies
- Familial focal epilepsy with variable foci
- Familial hemiplegic migraine
- Familial paroxysmal kinesigenic dyskinesia
- Fatal familial insomnia
- Fatty acid hydroxylase-associated neurodegeneration
- FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
- FOXG1 syndrome
- FOXP1 Syndrome
- Fragile X-associated tremor/ataxia syndrome
- Friedreich Ataxia
- Frontotemporal dementia with motor neuron disease
- Frontotemporal dementia with parkinsonism-17
G
H
- Hemorrhagic Stroke
- Hereditary cerebral amyloid angiopathy
- Hereditary hyperekplexia
- Hereditary motor and sensory neuropathy, Okinawa type
- Hereditary myopathy with early respiratory failure
- Hereditary neuropathy with liability to pressure palsies
- Hereditary sensory and autonomic neuropathy type IE
- Hereditary sensory and autonomic neuropathy type II
- Hereditary sensory and autonomic neuropathy type V
- Hereditary sensory neuropathy type IA
- Huntington disease-like 1
- Huntington's Disease
- Huntington's disease-like
- Hyperkalemic periodic paralysis
- Hypermanganesemia with dystonia
- Hypokalemic periodic paralysis
- Hypomyelination with brainstem and spinal cord involvement and leg spasticity
I
- Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
- Infantile neuroaxonal dystrophy
- Infantile-onset ascending hereditary spastic paralysis
- Infantile-onset spinocerebellar ataxia
- Insomnia
- Intellectual disability-cataracts-calcified pinnae-myopathy syndrome
- Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome
- Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome
- Intellectual disability-strabismus syndrome
- Ischemic Stroke
- Isolated lissencephaly sequence
J
L
- Lafora progressive myoclonus epilepsy
- Laing distal myopathy
- LAMA2-related muscular dystrophy
- Lennox-Gastaut syndrome
- Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
- Leukoencephalopathy with calcifications and cysts
- Leukoencephalopathy with thalamus and brainstem involvement and high lactate
- Leukoencephalopathy with vanishing white matter
- Lewy Body Dementia
- Limb-girdle muscular dystrophy
- Lissencephaly with cerebellar hypoplasia
- LMNA-related congenital muscular dystrophy
M
- Marinesco-Sjögren syndrome
- McLeod neuroacanthocytosis syndrome
- MECP2-related severe neonatal encephalopathy
- Megalencephalic leukoencephalopathy with subcortical cysts
- Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome
- MEND syndrome
- Metachromatic leukodystrophy
- Microcephalic cortical malformations-short stature due to RTTN deficiency
- Microcephaly, seizures, and developmental delay
- Migraine
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
- Mitochondrial membrane protein-associated neurodegeneration
- Miyoshi myopathy
- Moyamoya disease
- Multiminicore disease
- Multiple mitochondrial dysfunctions syndrome type 3
- Multiple Sclerosis
- Multiple system atrophy
- Muscular Dystrophy
- Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
- Myasthenia Gravis
- Myoclonic epilepsy myopathy sensory ataxia
- Myoclonic epilepsy with ragged-red fibers
- Myoclonus-dystonia
- Myosin storage myopathy
- Myositis
- Myotonia congenita
- MYT1L-related developmental delay-intellectual disability-obesity syndrome
N
- Neuroferritinopathy
- Neurofibromatosis type 1
- Neuromyelitis optica
- Neutral lipid storage disease with myopathy
- Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy
- Non-specific early-onset epileptic encephalopathy
- Nonketotic hyperglycinemia
- Nonsyndromic holoprosencephaly
O
P
- Pantothenate kinase-associated neurodegeneration
- Paralysis
- Paramyotonia congenita
- Parkinson's Disease
- Paroxysmal extreme pain disorder
- Pelizaeus-Merzbacher disease
- Perry syndrome
- Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome
- PRICKLE1-related progressive myoclonus epilepsy with ataxia
- Primary familial brain calcification
- Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome
- Progressive encephalopathy with leukodystrophy due to DECR deficiency
- Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome
- Progressive myoclonic epilepsy type 1
- Progressive Supranuclear Palsy
- PRUNE1-related neurological syndrome
- Pyridoxal phosphate-responsive seizures
- Pyridoxine-dependent epilepsy
R
- Rapid-onset dystonia parkinsonism
- Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome
- Restless Legs
- Restless legs syndrome
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
- Rett Syndrome
- Reye Syndrome
- Rigid spine muscular dystrophy
- Rippling muscle disease
- RNAse T2-deficient leukoencephalopathy
S
- Sciatica
- SCN8A-related epilepsy with encephalopathy
- Seizures
- Sepiapterin reductase deficiency
- SETBP1 haploinsufficiency disorder
- Silver syndrome
- Small fiber neuropathy
- Spastic paraplegia type 2
- Spastic paraplegia type 7
- Spina Bifida
- Spinal and bulbar muscular atrophy
- Spinal Cord Injuries
- Spinal Muscular Atrophy
- Spinal muscular atrophy with lower extremity predominance
- Spinal muscular atrophy with progressive myoclonic epilepsy
- Spinal muscular atrophy with respiratory distress type 1
- Spinocerebellar ataxia type 1
- Spinocerebellar ataxia type 2
- Spinocerebellar ataxia type 3
- Spinocerebellar ataxia type 36
- Spinocerebellar ataxia type 6
- Sporadic hemiplegic migraine
- SSR4-CDG
- Stroke
- Stuttering
- STXBP1 encephalopathy
- Syringomyelia