Nervous system disorder

Part of

Sub-types of Nervous system disorder

• Central nervous system disorder 119 trials · 20,455 incl. sub-types
  19 sub-types

  • Brain disorder 137 trials · 16,709 incl. sub-types Sub-types →
  • Neurodegenerative disease 187 trials · 3,289 incl. sub-types Sub-types →
  • Central nervous system neoplasm 51 trials · 1,986 incl. sub-types Sub-types →
  • Spinal cord disorder 47 trials · 1,255 incl. sub-types Sub-types →
  • Autoimmune disorder of central nervous system 2 trials · 881 incl. sub-types Sub-types →
  • Palsy 36 trials · 846 incl. sub-types Sub-types →
  • Encephalomyelitis 3 trials · 227 incl. sub-types Sub-types →
  • Autonomic nervous system disorder 59 trials · 209 incl. sub-types Sub-types →
  • Central nervous system infectious disorder 10 trials · 163 incl. sub-types Sub-types →
  • Optic nerve disorder 23 trials · 96 incl. sub-types Sub-types →
  • Tinnitus 91 trials
  • Central nervous system vasculitis 3 trials · 55 incl. sub-types Sub-types →
  • Trigeminal neuralgia 37 trials
  • Cerebrospinal fluid leak 16 trials · 17 incl. sub-types Sub-types →
  • High pressure neurological syndrome 0 trials · 5 incl. sub-types Sub-types →
  • SPAST-related motor disorder 0 trials · 2 incl. sub-types Sub-types →
  • Congenital narrowing of cervical spinal canal 0 trials
  • Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly 0 trials
  • Sporadic fetal brain disruption sequence 0 trials Sub-types →
• Hereditary neurological disease 6 trials · 5,791 incl. sub-types
  264 sub-types

  • Parkinson disease 1,169 trials · 1,296 incl. sub-types Sub-types →
  • Anxiety 1,036 trials
  • Hereditary neuromuscular disease 3 trials · 935 incl. sub-types Sub-types →
  • Inherited neurodegenerative disorder 11 trials · 808 incl. sub-types Sub-types →
  • Inherited retinal dystrophy 41 trials · 513 incl. sub-types Sub-types →
  • Mendelian neurodevelopmental disorder 0 trials · 208 incl. sub-types Sub-types →
  • Obsessive-compulsive disorder 197 trials
  • Hereditary ataxia 2 trials · 119 incl. sub-types Sub-types →
  • Essential tremor 102 trials · 104 incl. sub-types Sub-types →
  • Neurofibromatosis 19 trials · 94 incl. sub-types Sub-types →
  • Myalgic encephalomeyelitis/chronic fatigue syndrome 75 trials
  • Inherited orthostatic hypotension 0 trials · 71 incl. sub-types Sub-types →
  • Nonsyndromic genetic hearing loss 4 trials · 67 incl. sub-types Sub-types →
  • Inherited vitreoretinopathy 0 trials · 58 incl. sub-types Sub-types →
  • Paraganglioma 53 trials · 57 incl. sub-types Sub-types →
  • Retinal detachment 28 trials · 52 incl. sub-types Sub-types →
  • Tuberous sclerosis 41 trials · 44 incl. sub-types Sub-types →
  • Combined pituitary hormone deficiencies, genetic form 1 trial · 42 incl. sub-types Sub-types →
  • Endogenous depression 42 trials
  • Specific phobia 22 trials · 42 incl. sub-types Sub-types →
  • Tourette syndrome 41 trials
  • Familial partial epilepsy 0 trials · 39 incl. sub-types Sub-types →
  • Cerebral lipidosis with dementia 0 trials · 38 incl. sub-types Sub-types →
  • Inherited dystonia 0 trials · 36 incl. sub-types Sub-types →
  • Normal pressure hydrocephalus 36 trials
  • Mismatch repair cancer syndrome 1 34 trials
  • Hereditary generalized epilepsy 0 trials · 33 incl. sub-types Sub-types →
  • X-linked deafness 0 trials · 32 incl. sub-types Sub-types →
  • Familial isolated pituitary adenoma 1 trial · 31 incl. sub-types Sub-types →
  • Von Hippel-Lindau disease 27 trials
  • Specific language impairment 26 trials Sub-types →
  • Stutter disorder 22 trials Sub-types →
  • Moyamoya disease 20 trials Sub-types →
  • Angelman syndrome 19 trials Sub-types →
  • Cerebral amyloid angiopathy 16 trials · 17 incl. sub-types Sub-types →
  • Li-Fraumeni syndrome 16 trials
  • Childhood apraxia of speech 16 trials
  • Intracranial berry aneurysm 12 trials Sub-types →
  • Progressive myoclonus epilepsy 5 trials · 12 incl. sub-types Sub-types →
  • DiGeorge syndrome 11 trials
  • Auditory neuropathy 7 trials · 11 incl. sub-types Sub-types →
  • Major affective disorder 6 11 trials
  • Spastic quadriplegic cerebral palsy 10 trials Sub-types →
  • Chiari malformation type I 9 trials
  • Neurohypophyseal diabetes insipidus 9 trials
  • Sturge-Weber syndrome 8 trials
  • Progressive external ophthalmoplegia 4 trials · 8 incl. sub-types Sub-types →
  • Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan 0 trials · 8 incl. sub-types Sub-types →
  • Red-green color blindness 7 trials
  • Duane retraction syndrome 6 trials Sub-types →
  • Arthrogryposis 4 trials · 6 incl. sub-types Sub-types →
  • Inborn aminoacylase deficiency 0 trials · 6 incl. sub-types Sub-types →
  • Undetermined early-onset epileptic encephalopathy 1 trial · 6 incl. sub-types Sub-types →
  • GLUT1 deficiency syndrome 4 trials · 5 incl. sub-types Sub-types →
  • Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease 5 trials
  • Congenital nystagmus 4 trials · 5 incl. sub-types Sub-types →
  • Congenital stationary night blindness 2 trials · 5 incl. sub-types Sub-types →
  • Narcolepsy 1 5 trials
  • Nevoid basal cell carcinoma syndrome 5 trials Sub-types →
  • Qualitative or quantitative defects of beta-sarcoglycan 0 trials · 5 incl. sub-types Sub-types →
  • TTN-related myopathy 2 trials · 4 incl. sub-types Sub-types →
  • Corpus callosum, agenesis of 4 trials Sub-types →
  • Glutaryl-CoA dehydrogenase deficiency 4 trials
  • Qualitative or quantitative defects of gamma-sarcoglycan 1 trial · 4 incl. sub-types Sub-types →
  • Velocardiofacial syndrome 4 trials
  • Hoyeraal-Hreidarsson syndrome 3 trials
  • Riley-Day syndrome 3 trials
  • TPM2-related myopathy 1 trial · 3 incl. sub-types Sub-types →
  • Bilirubin encephalopathy 3 trials Sub-types →
  • Central nervous system lupus 3 trials
  • Congenital hydrocephalus 1 trial · 3 incl. sub-types Sub-types →
  • Encephalopathy, acute, infection-induced 2 trials · 3 incl. sub-types Sub-types →
  • Familial congenital mirror movements 3 trials Sub-types →
  • Familial porencephaly 0 trials · 3 incl. sub-types Sub-types →
  • Inherited reflex epilepsy 0 trials · 3 incl. sub-types Sub-types →
  • Megalencephaly-capillary malformation-polymicrogyria syndrome 3 trials
  • Neuromuscular disease caused by qualitative or quantitative defects of dysferlin 0 trials · 3 incl. sub-types Sub-types →
  • Pontocerebellar hypoplasia 1 trial · 3 incl. sub-types Sub-types →
  • Pyridoxine-dependent epilepsy 3 trials Sub-types →
  • Qualitative or quantitative defects of alpha-sarcoglycan 0 trials · 3 incl. sub-types Sub-types →
  • ATP1A3-associated neurological disorder 0 trials · 2 incl. sub-types Sub-types →
  • Chiari malformation type II 2 trials
  • PAX6-related ocular dysgenesis 0 trials · 2 incl. sub-types Sub-types →
  • SPAST-related motor disorder 0 trials · 2 incl. sub-types Sub-types →
  • Childhood-onset nemaline myopathy 1 trial · 2 incl. sub-types Sub-types →
  • Choroid plexus papilloma 2 trials
  • Dyskinesia with orofacial involvement, autosomal dominant 2 trials
  • Hereditary retinoblastoma 2 trials
  • Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome 2 trials
  • Isolated hereditary congenital facial paralysis 2 trials Sub-types →
  • Leukoencephalopathy, megalencephalic 0 trials · 2 incl. sub-types Sub-types →
  • Pyridoxal phosphate-responsive seizures 2 trials
  • Qualitative or quantitative defects of delta-sarcoglycan 0 trials · 2 incl. sub-types Sub-types →
  • Retinal ciliopathy 0 trials · 2 incl. sub-types Sub-types →
  • 2-hydroxyglutaric aciduria 0 trials · 1 incl. sub-types Sub-types →
  • Brown syndrome 1 trial
  • Gerstmann-Straussler-Scheinker syndrome 1 trial
  • Guillain-Barre syndrome, familial 1 trial
  • PRRT2-associated paroxysmal movement disorder 0 trials · 1 incl. sub-types Sub-types →
  • TH-deficient dopa-responsive dystonia 1 trial
  • TPM3-related myopathy 1 trial Sub-types →
  • Anencephaly 1 trial Sub-types →
  • Bilateral striopallidodentate calcinosis 1 trial Sub-types →
  • Biotin-responsive basal ganglia disease 1 trial
  • Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 1 trial
  • Coloboma of optic nerve 1 trial Sub-types →
  • Dilated cardiomyopathy 3B 1 trial
  • Epilepsy with myoclonic atonic seizures 1 trial
  • Familial hemiplegic migraine 0 trials · 1 incl. sub-types Sub-types →
  • Familial meningioma 1 trial
  • Familial periodic paralysis 0 trials · 1 incl. sub-types Sub-types →
  • Familial pterygium of the conjunctiva 1 trial
  • Famililal cerebral cavernous malformations 1 trial Sub-types →
  • Iris hypoplasia with glaucoma 1 trial
  • Isolated cerebellar hypoplasia/agenesis 1 trial
  • Linear nevus sebaceous syndrome 1 trial
  • Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome 1 trial
  • Multiminicore myopathy 1 trial Sub-types →
  • Myoclonus, familial 1 trial Sub-types →
  • Myopathy caused by variation in POMGNT1 0 trials · 1 incl. sub-types Sub-types →
  • Neurocutaneous melanocytosis 1 trial
  • Neuromuscular disease caused by qualitative or quantitative defects of plectin 0 trials · 1 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of telethonin 0 trials · 1 incl. sub-types Sub-types →
  • Qualitative or quantitative defects of desmin 0 trials · 1 incl. sub-types Sub-types →
  • Rhabdoid tumor predisposition syndrome 2 1 trial
  • Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked 1 trial
  • Severe congenital nemaline myopathy 0 trials · 1 incl. sub-types Sub-types →
  • B4GALT1-congenital disorder of glycosylation 0 trials
  • Bailey-Bloch congenital myopathy 0 trials
  • Behr syndrome 0 trials
  • Behrens Baumann dust syndrome 0 trials
  • Brody myopathy 0 trials
  • DHDDS-related syndrome 0 trials Sub-types →
  • Frey syndrome 0 trials
  • Griscelli syndrome type 1 0 trials
  • HSD10 mitochondrial disease 0 trials Sub-types →
  • Johanson-Blizzard syndrome 0 trials
  • KIF5A-related neurological disorder 0 trials Sub-types →
  • LSM7-related leukodystrophy and cerebellar atrophy 0 trials
  • Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome 0 trials
  • NPHP3-related Meckel-like syndrome 0 trials
  • PEHO-like syndrome 0 trials
  • PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome 0 trials
  • PrP systemic amyloidosis 0 trials
  • Prader-Willi-like syndrome 0 trials Sub-types →
  • Ritscher-Schinzel syndrome 0 trials Sub-types →
  • SERAC1-related neurological disorder 0 trials Sub-types →
  • SLC39A8-CDG 0 trials
  • SLC6A3-related dopamine transporter deficiency syndrome 0 trials Sub-types →
  • TELO2-related intellectual disability-neurodevelopmental disorder 0 trials
  • TUBB3-related tubulinopathy 0 trials Sub-types →
  • Uner Tan Syndrome 0 trials
  • VPS11-related neurological disorder 0 trials Sub-types →
  • Valence-Farazi cerebellar ataxia syndrome 0 trials
  • X-linked immunoneurologic disorder 0 trials
  • X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome 0 trials
  • Achromatopsia 6 0 trials
  • Adult-onset nemaline myopathy 0 trials
  • Age-related hearing impairment 1 0 trials
  • Age-related hearing impairment 2 0 trials
  • Alpha-actinopathy 0 trials Sub-types →
  • Angioid streaks 0 trials Sub-types →
  • Aniridia 2 0 trials
  • Aniridia 3 0 trials
  • Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome 0 trials
  • Band heterotopia of brain 0 trials
  • Benign familial infantile epilepsy 0 trials Sub-types →
  • Benign neonatal seizures 0 trials Sub-types →
  • Bilateral frontoparietal polymicrogyria 0 trials
  • Bilateral generalized polymicrogyria 0 trials
  • Bilateral parasagittal parieto-occipital polymicrogyria 0 trials
  • Blue color blindness 0 trials
  • Bradyopsia 0 trials Sub-types →
  • Brain malformations with or without urinary tract defects 0 trials
  • Brain-lung-thyroid syndrome 0 trials
  • Cathepsin a-related arteriopathy-strokes-leukoencephalopathy 0 trials
  • Caveolinopathy 0 trials Sub-types →
  • Cerebellar-facial-dental syndrome 0 trials
  • Chorea, remitting, with nystagmus and cataract 0 trials
  • Choreoathetosis, familial inverted 0 trials
  • Cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome 0 trials
  • Cluster headache, familial 0 trials
  • Complex cortical dysplasia with other brain malformations 0 trials Sub-types →
  • Congenital insensitivity to pain with severe intellectual disability 0 trials
  • Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome 0 trials
  • Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive 0 trials
  • Encephalopathy due to mitochondrial and peroxisomal fission defect 0 trials Sub-types →
  • Encephalopathy, acute transient 0 trials
  • Encephalopathy, recurrent, of childhood 0 trials
  • Epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features 0 trials Sub-types →
  • Epilepsy, familial adult myoclonic 0 trials Sub-types →
  • Familial Alzheimer-like prion disease 0 trials
  • Familial congenital palsy of trochlear nerve 0 trials
  • Familial hemophagocytic lymphohistiocytosis type 1 0 trials
  • Familial hyperprolactinemia 0 trials
  • Familial infantile myoclonic epilepsy 0 trials
  • Familial panic disorder 0 trials Sub-types →
  • Familial retinal arterial macroaneurysm 0 trials
  • Familial schizencephaly 0 trials
  • Familial syringomyelia 0 trials
  • Fatty acyl-CoA reductase 1 upregulation 0 trials
  • Febrile seizures, familial, 11 0 trials
  • Folinic acid-responsive seizures 0 trials
  • Glycine encephalopathy 0 trials Sub-types →
  • Hereditary hyperekplexia 0 trials Sub-types →
  • Hereditary progressive chorea without dementia 0 trials
  • Holoprosencephaly 0 trials Sub-types →
  • Hyperlexia 0 trials
  • Hypermanganesemia with dystonia 2 0 trials
  • Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly 0 trials
  • Infection-induced acute-onset axonal neuropathy 0 trials
  • Intracranial extraskeletal myxoid chondrosarcoma 0 trials
  • Lateral meningocele syndrome 0 trials
  • Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome 0 trials
  • Lissencephaly spectrum disorders 0 trials Sub-types →
  • Macrocephaly/megalencephaly syndrome, autosomal recessive 0 trials
  • Major affective disorder 1 0 trials
  • Major affective disorder 2 0 trials
  • Major affective disorder 3 0 trials
  • Major affective disorder 4 0 trials
  • Major affective disorder 5 0 trials
  • Major affective disorder 7 0 trials
  • Major affective disorder 8 0 trials
  • Major affective disorder 9 0 trials
  • Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome 0 trials Sub-types →
  • Melanoma and neural system tumor syndrome 0 trials
  • Microangiopathy and leukoencephalopathy, pontine, autosomal dominant 0 trials
  • Microcephaly-complex motor and sensory axonal neuropathy syndrome 0 trials
  • Multiple pterygium-malignant hyperthermia syndrome 0 trials
  • Myofibrillar myopathy 5 0 trials
  • Myopathy due to calsequestrin and SERCA1 protein overload 0 trials
  • Myopic macular degeneration 0 trials
  • Myosclerosis 0 trials
  • Narcolepsy 3 0 trials
  • Narcolepsy 7 0 trials
  • Neuromuscular disease caused by qualitative or quantitative defects of TRIM32 0 trials Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7) 0 trials Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of perlecan 0 trials Sub-types →
  • Neuroocular syndrome 0 trials Sub-types →
  • Occipital pachygyria and polymicrogyria 0 trials
  • Oculocerebrocutaneous syndrome 0 trials
  • Orofaciodigital syndrome type 6 0 trials
  • Parietal foramina 0 trials Sub-types →
  • Parkinsonism with polyneuropathy 0 trials
  • Paroxysmal extreme pain disorder 0 trials
  • Periventricular nodular heterotopia 0 trials Sub-types →
  • Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome 0 trials
  • Phakomatosis pigmentokeratotica 0 trials
  • Polyhydramnios, megalencephaly, and symptomatic epilepsy 0 trials
  • Polymicrogyria, bilateral perisylvian, autosomal recessive 0 trials
  • Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis 0 trials
  • Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome 0 trials
  • Prosopagnosia, hereditary 0 trials
  • Proximal myopathy with extrapyramidal signs 0 trials
  • Red color blindness 0 trials
  • Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome 0 trials
  • Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome 0 trials
  • Schizophrenia 15 0 trials
  • Schizophrenia 16 0 trials
  • Schizophrenia 19 0 trials
  • Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome 0 trials
  • Severe neonatal-onset encephalopathy with microcephaly 0 trials
  • Spongiform encephalopathy with neuropsychiatric features 0 trials
  • Typical nemaline myopathy 0 trials Sub-types →
• Neurovascular disorder 5 trials · 4,209 incl. sub-types
  29 sub-types

  • Cerebrovascular disorder 108 trials · 3,292 incl. sub-types Sub-types →
  • Migraine disorder 393 trials · 414 incl. sub-types Sub-types →
  • Retinal vascular disorder 9 trials · 324 incl. sub-types Sub-types →
  • Intracranial hypertension 51 trials · 97 incl. sub-types Sub-types →
  • Central nervous system vasculitis 3 trials · 55 incl. sub-types Sub-types →
  • Trigeminal autonomic cephalalgia 8 trials · 27 incl. sub-types Sub-types →
  • Choroid plexus cancer 0 trials · 11 incl. sub-types Sub-types →
  • Choroid cancer 0 trials · 10 incl. sub-types Sub-types →
  • Hemangioblastoma 9 trials · 10 incl. sub-types Sub-types →
  • Lymphatic malformation 5 8 trials
  • Choroideremia 6 trials Sub-types →
  • Ornithine aminotransferase deficiency 4 trials
  • Benign choroid plexus neoplasm 0 trials · 2 incl. sub-types Sub-types →
  • Cavernous sinus meningioma 2 trials
  • Central nervous system hemangioma 0 trials · 2 incl. sub-types Sub-types →
  • Hemangioma of retina 0 trials · 1 incl. sub-types Sub-types →
  • Retinal ischemia 1 trial
  • Norman-Roberts syndrome 0 trials
  • Wyburn-Mason syndrome 0 trials
  • Benign neoplasm of choroid 0 trials Sub-types →
  • Central nervous system angiosarcoma 0 trials
  • Choroidal dystrophy, central areolar 2 0 trials
  • Choroidal dystrophy, central areolar, 1 0 trials
  • Choroidal sclerosis 0 trials Sub-types →
  • Eyelid capillary hemangioma 0 trials
  • Malignant jugulotympanic paraganglioma 0 trials
  • Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability 0 trials
  • Neoplasm of aortic body 0 trials
  • Retinal dystrophies primarily involving Bruch's membrane 0 trials Sub-types →
• Nervous system neoplasm 8 trials · 2,587 incl. sub-types
  7 sub-types

  • Nervous system cancer 17 trials · 2,003 incl. sub-types Sub-types →
  • Central nervous system neoplasm 51 trials · 1,986 incl. sub-types Sub-types →
  • Neuroepithelial neoplasm 6 trials · 1,344 incl. sub-types Sub-types →
  • Peripheral nervous system neoplasm 3 trials · 197 incl. sub-types Sub-types →
  • Tumor of cranial and spinal nerves 0 trials · 129 incl. sub-types Sub-types →
  • Nervous system benign neoplasm 0 trials · 87 incl. sub-types Sub-types →
  • Retina neoplasm 2 trials · 36 incl. sub-types Sub-types →
• Perceptual disorders 22 trials · 2,391 incl. sub-types
  9 sub-types

  • Agnosia 839 trials · 857 incl. sub-types Sub-types →
  • Hearing disorder 24 trials · 533 incl. sub-types Sub-types →
  • Inherited retinal dystrophy 41 trials · 513 incl. sub-types Sub-types →
  • Vision disorder 105 trials · 382 incl. sub-types Sub-types →
  • Vestibular disorder 64 trials · 92 incl. sub-types Sub-types →
  • Apraxia 17 trials · 40 incl. sub-types Sub-types →
  • Auditory perceptual disorders 12 trials · 22 incl. sub-types Sub-types →
  • Hallucinogen-persisting perception disorder 4 trials
  • Allesthesia 1 trial
• Neuromuscular disease 112 trials · 2,353 incl. sub-types
  8 sub-types

  • Peripheral neuropathy 93 trials · 1,473 incl. sub-types Sub-types →
  • Hereditary neuromuscular disease 3 trials · 935 incl. sub-types Sub-types →
  • Motor neuron disorder 70 trials · 510 incl. sub-types Sub-types →
  • Vestibular disorder 64 trials · 92 incl. sub-types Sub-types →
  • Muscular channelopathy 0 trials · 19 incl. sub-types Sub-types →
  • Atrophic muscular disease 7 trials
  • Neuromuscular junction disease 1 trial · 7 incl. sub-types Sub-types →
  • Akinetopsia 0 trials
• Peripheral nervous system disorder 121 trials · 2,293 incl. sub-types
  18 sub-types

  • Peripheral neuropathy 93 trials · 1,473 incl. sub-types Sub-types →
  • Autonomic nervous system disorder 59 trials · 209 incl. sub-types Sub-types →
  • Peripheral nervous system neoplasm 3 trials · 197 incl. sub-types Sub-types →
  • Autoimmune disorder of peripheral nervous system 0 trials · 195 incl. sub-types Sub-types →
  • Radiculopathy 163 trials
  • Third cranial nerve disorder 1 trial · 87 incl. sub-types Sub-types →
  • Trigeminal nerve disorder 3 trials · 63 incl. sub-types Sub-types →
  • Facial nerve disorder 4 trials · 53 incl. sub-types Sub-types →
  • Neuroma 20 trials · 27 incl. sub-types Sub-types →
  • Olfactory nerve disorder 8 trials · 12 incl. sub-types Sub-types →
  • Vestibulocochlear nerve disorder 2 trials · 11 incl. sub-types Sub-types →
  • Glossopharyngeal nerve disorder 2 trials · 8 incl. sub-types Sub-types →
  • Abducens nerve disorder 0 trials · 2 incl. sub-types Sub-types →
  • Cauda equina syndrome 2 trials Sub-types →
  • Accessory nerve disorder 1 trial Sub-types →
  • Hypoglossal nerve disorder 1 trial Sub-types →
  • Trochlear nerve disorder 1 trial Sub-types →
  • Peroneal nerve paralysis 0 trials
• Neurological pain disorder 1 trial · 1,839 incl. sub-types
  9 sub-types

  • Chronic pain syndrome 673 trials · 976 incl. sub-types Sub-types →
  • Headache disorder 119 trials · 491 incl. sub-types Sub-types →
  • Neuralgia 238 trials · 384 incl. sub-types Sub-types →
  • Psychologic dyspareunia 31 trials
  • Coccygodynia 19 trials
  • Vulvodynia 18 trials
  • Eagle syndrome 0 trials
  • Glossodynia 0 trials
  • Paroxysmal extreme pain disorder 0 trials
• Nervous system injury 24 trials · 1,318 incl. sub-types
  2 sub-types

  • Brain injury 220 trials · 693 incl. sub-types Sub-types →
  • Spinal cord injury 650 trials
• Neurodevelopmental disorder 161 trials · 1,133 incl. sub-types
  18 sub-types

  • Complex neurodevelopmental disorder 3 trials · 875 incl. sub-types Sub-types →
  • Mendelian neurodevelopmental disorder 0 trials · 208 incl. sub-types Sub-types →
  • Intellectual disability 138 trials · 175 incl. sub-types Sub-types →
  • Williams syndrome 18 trials
  • Microcephaly 4 trials · 13 incl. sub-types Sub-types →
  • Atypical Rett syndrome 0 trials · 12 incl. sub-types Sub-types →
  • Alternating hemiplegia 0 trials · 3 incl. sub-types Sub-types →
  • Aicardi syndrome 2 trials
  • Hao-Fountain syndrome 0 trials Sub-types →
  • TCF7L2-related neurodevelopmental disorder 0 trials
  • Yoon-Bellen neurodevelopmental syndrome 0 trials
  • Neurodevelopmental disorder with microcephaly, hypotonia, and absent language 0 trials
  • Neurodevelopmental disorder with parkinsonism or other movement abnormalities 0 trials
  • Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies 0 trials
  • Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss 0 trials
  • Neurodevelopmental disorder with seizures and brain abnormalities 0 trials
  • Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome 0 trials Sub-types →
  • Toluene embryopathy 0 trials
• Autoimmune disorder of the nervous system 47 trials · 1,067 incl. sub-types
  4 sub-types

  • Autoimmune disorder of central nervous system 2 trials · 881 incl. sub-types Sub-types →
  • Autoimmune disorder of peripheral nervous system 0 trials · 195 incl. sub-types Sub-types →
  • Pediatric acute-onset neuropsychiatric syndrome 8 trials · 10 incl. sub-types Sub-types →
  • Autoimmune retinopathy 0 trials
• Retinal disorder 89 trials · 963 incl. sub-types
  32 sub-types

  • Retinal degeneration 41 trials · 576 incl. sub-types Sub-types →
  • Retinal vascular disorder 9 trials · 324 incl. sub-types Sub-types →
  • Inherited vitreoretinopathy 0 trials · 58 incl. sub-types Sub-types →
  • Retinal detachment 28 trials · 52 incl. sub-types Sub-types →
  • Retina neoplasm 2 trials · 36 incl. sub-types Sub-types →
  • Retinal edema 1 trial · 29 incl. sub-types Sub-types →
  • Macular holes 19 trials
  • Night blindness 5 trials · 10 incl. sub-types Sub-types →
  • Retinitis 1 trial · 10 incl. sub-types Sub-types →
  • Central serous chorioretinopathy 8 trials
  • Proliferative vitreoretinopathy 7 trials Sub-types →
  • Achromatopsia 4 trials · 6 incl. sub-types Sub-types →
  • Retinal ciliopathy 0 trials · 2 incl. sub-types Sub-types →
  • Hypertensive retinopathy 1 trial
  • Iris hypoplasia with glaucoma 1 trial
  • Retinal ischemia 1 trial
  • Retinal nerve fiber layer disorder 1 trial Sub-types →
  • Eales disease 0 trials
  • Acute macular neuroretinopathy 0 trials
  • Angioid streaks 0 trials Sub-types →
  • Autoimmune retinopathy 0 trials
  • Bradyopsia 0 trials Sub-types →
  • Cancer-associated retinopathy 0 trials
  • Congenital retinal arteriovenous communication 0 trials
  • Isolated chorioretinal dystrophy 0 trials
  • Isolated foveal hypoplasia 0 trials
  • Melanoma associated retinopathy 0 trials
  • Myopic macular degeneration 0 trials
  • Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome 0 trials
  • Persistent placoid maculopathy 0 trials
  • Rubeosis iridis 0 trials
  • Torpedo maculopathy 0 trials
• Movement disorder 108 trials · 805 incl. sub-types
  54 sub-types

  • Extrapyramidal and movement disease 0 trials · 149 incl. sub-types Sub-types →
  • Cerebellar ataxia 40 trials · 144 incl. sub-types Sub-types →
  • Multiple system atrophy 110 trials · 119 incl. sub-types Sub-types →
  • Essential tremor 102 trials · 104 incl. sub-types Sub-types →
  • Progressive supranuclear palsy 74 trials · 78 incl. sub-types Sub-types →
  • Huntington disease 76 trials Sub-types →
  • Progressive non-fluent aphasia 24 trials · 44 incl. sub-types Sub-types →
  • Behavioral variant of frontotemporal dementia 22 trials · 42 incl. sub-types Sub-types →
  • Tourette syndrome 41 trials
  • Corticobasal syndrome 20 trials
  • Frontotemporal dementia with motor neuron disease 14 trials · 19 incl. sub-types Sub-types →
  • Chronic tic disorder 15 trials
  • Choreatic disease 11 trials Sub-types →
  • Neurodegeneration with brain iron accumulation 1 trial · 8 incl. sub-types Sub-types →
  • Arthrogryposis 4 trials · 6 incl. sub-types Sub-types →
  • Inherited Creutzfeldt-Jakob disease 5 trials
  • Primary orthostatic tremor 5 trials
  • Clonic hemifacial spasm 4 trials
  • Familial congenital mirror movements 3 trials Sub-types →
  • Transient tic disorder 3 trials
  • Dyskinesia with orofacial involvement, autosomal dominant 2 trials
  • Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome 2 trials
  • Opsoclonus-myoclonus syndrome 2 trials
  • Lafora disease 1 trial Sub-types →
  • PRRT2-associated paroxysmal movement disorder 0 trials · 1 incl. sub-types Sub-types →
  • Unverricht-Lundborg syndrome 1 trial
  • Benign shuddering attacks 1 trial
  • Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 1 trial
  • Intellectual disability-hyperkinetic movement-truncal ataxia syndrome 0 trials · 1 incl. sub-types Sub-types →
  • Myoclonus, familial 1 trial Sub-types →
  • Neuronal intranuclear inclusion disease 1 trial
  • Psychogenic movement disorders 1 trial
  • Huntington disease-like 3 0 trials
  • Huntington disease-like syndrome due to C9ORF72 expansions 0 trials
  • SLC6A3-related dopamine transporter deficiency syndrome 0 trials Sub-types →
  • Sandifer syndrome 0 trials
  • Benign paroxysmal tonic upgaze of childhood with ataxia 0 trials
  • Brain-lung-thyroid syndrome 0 trials
  • Childhood-onset benign chorea with striatal involvement 0 trials
  • Complex movement disorder with or without neurodevelopmental features 0 trials Sub-types →
  • Epilepsy with myoclonic absences 0 trials
  • Hereditary geniospasm 0 trials
  • Hyperekplexia 0 trials Sub-types →
  • Isolated facial myokymia 0 trials
  • Kuru 0 trials
  • Lingual-facial-buccal dyskinesia 0 trials
  • Neuroacanthocytosis 0 trials Sub-types →
  • Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome 0 trials
  • Progressive myoclonic epilepsy type 7 0 trials
  • Proximal myopathy with extrapyramidal signs 0 trials
  • Sensorineural hearing loss-early graying-essential tremor syndrome 0 trials
  • Spinal muscular atrophy-progressive myoclonic epilepsy syndrome 0 trials
  • Tremor-nystagmus-duodenal ulcer syndrome 0 trials
  • Variably protease-sensitive prionopathy 0 trials
• Cranial nerve neuropathy 4 trials · 392 incl. sub-types
  17 sub-types

  • Cranial nerve palsy 2 trials · 122 incl. sub-types Sub-types →
  • Optic nerve disorder 23 trials · 96 incl. sub-types Sub-types →
  • Third cranial nerve disorder 1 trial · 87 incl. sub-types Sub-types →
  • Ocular motility disease 4 trials · 65 incl. sub-types Sub-types →
  • Trigeminal nerve disorder 3 trials · 63 incl. sub-types Sub-types →
  • Cranial neuralgia 0 trials · 53 incl. sub-types Sub-types →
  • Facial nerve disorder 4 trials · 53 incl. sub-types Sub-types →
  • Olfactory nerve disorder 8 trials · 12 incl. sub-types Sub-types →
  • Vestibulocochlear nerve disorder 2 trials · 11 incl. sub-types Sub-types →
  • Cranial nerve neoplasm 0 trials · 8 incl. sub-types Sub-types →
  • Glossopharyngeal nerve disorder 2 trials · 8 incl. sub-types Sub-types →
  • Abducens nerve disorder 0 trials · 2 incl. sub-types Sub-types →
  • Jaw-winking syndrome 2 trials Sub-types →
  • Accessory nerve disorder 1 trial Sub-types →
  • Hypoglossal nerve disorder 1 trial Sub-types →
  • Trochlear nerve disorder 1 trial Sub-types →
  • Pseudobulbar palsy 0 trials
• Congenital nervous system disorder 1 trial · 287 incl. sub-types
  217 sub-types

  • Spina bifida 44 trials · 59 incl. sub-types Sub-types →
  • Combined pituitary hormone deficiencies, genetic form 1 trial · 42 incl. sub-types Sub-types →
  • Prader-Willi syndrome 32 trials Sub-types →
  • 22q11.2 deletion syndrome 7 trials · 13 incl. sub-types Sub-types →
  • Leber congenital amaurosis 11 trials · 13 incl. sub-types Sub-types →
  • Congenital muscular dystrophy 1 trial · 10 incl. sub-types Sub-types →
  • Chediak-Higashi syndrome 9 trials
  • Congenital laryngeal palsy 9 trials
  • Congenital myotonic dystrophy 9 trials
  • Congenital vitreoretinal dysplasia 0 trials · 9 incl. sub-types Sub-types →
  • Progressive external ophthalmoplegia 4 trials · 8 incl. sub-types Sub-types →
  • Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan 0 trials · 8 incl. sub-types Sub-types →
  • RYR1-related myopathy 5 trials · 6 incl. sub-types Sub-types →
  • MERRF syndrome 5 trials
  • Smith-Magenis syndrome 5 trials
  • Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease 5 trials
  • Congenital nystagmus 4 trials · 5 incl. sub-types Sub-types →
  • TTN-related myopathy 2 trials · 4 incl. sub-types Sub-types →
  • Corpus callosum, agenesis of 4 trials Sub-types →
  • Mitochondrial neurogastrointestinal encephalomyopathy 4 trials Sub-types →
  • Severe intellectual disability-progressive spastic diplegia syndrome 4 trials
  • Rubinstein-Taybi syndrome 3 trials Sub-types →
  • TPM2-related myopathy 1 trial · 3 incl. sub-types Sub-types →
  • Cerebral cavernous malformation 3 trials Sub-types →
  • Congenital hydrocephalus 1 trial · 3 incl. sub-types Sub-types →
  • Congenital stationary night blindness autosomal dominant 1 3 trials
  • Familial congenital mirror movements 3 trials Sub-types →
  • Postsynaptic congenital myasthenic syndrome 0 trials · 3 incl. sub-types Sub-types →
  • Syndromic X-linked intellectual disability Lubs type 3 trials Sub-types →
  • FOXG1 disorder 2 trials
  • KBG syndrome 2 trials
  • Mobius syndrome 2 trials Sub-types →
  • Mowat-Wilson syndrome 2 trials Sub-types →
  • PHACE syndrome 2 trials
  • Childhood-onset nemaline myopathy 1 trial · 2 incl. sub-types Sub-types →
  • Congenital toxoplasmosis 2 trials
  • Isolated hereditary congenital facial paralysis 2 trials Sub-types →
  • Meningocele 2 trials Sub-types →
  • AICA-ribosiduria 1 trial
  • Bohring-Opitz syndrome 1 trial
  • Cohen syndrome 1 trial
  • Freeman-Sheldon syndrome 1 trial Sub-types →
  • Schuurs-Hoeijmakers syndrome 1 trial
  • TPM3-related myopathy 1 trial Sub-types →
  • Anencephaly 1 trial Sub-types →
  • Autism spectrum disorder due to AUTS2 deficiency 1 trial
  • Autosomal recessive limb-girdle muscular dystrophy type 2R1 1 trial
  • Autosomal recessive limb-girdle muscular dystrophy type 2Y 1 trial
  • Cephalocele 0 trials · 1 incl. sub-types Sub-types →
  • Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 1 trial
  • Chromosome 15q13.3 microdeletion syndrome 1 trial
  • Congenital contractural arachnodactyly 1 trial
  • Congenital stationary night blindness autosomal dominant 2 1 trial
  • Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome 1 trial
  • Isolated cerebellar hypoplasia/agenesis 1 trial
  • Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome 1 trial
  • Myopathy caused by variation in POMGNT1 0 trials · 1 incl. sub-types Sub-types →
  • Neuropathy, congenital hypomelinating 0 trials · 1 incl. sub-types Sub-types →
  • Polymicrogyria 1 trial Sub-types →
  • Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 1 trial Sub-types →
  • Severe congenital nemaline myopathy 0 trials · 1 incl. sub-types Sub-types →
  • Syndromic X-linked intellectual disability 5 1 trial
  • 3q27.3 microdeletion syndrome 0 trials
  • 7p22.1 microduplication syndrome 0 trials
  • 9q31.1q31.3 microdeletion syndrome 0 trials
  • 9q33.3q34.11 microdeletion syndrome 0 trials
  • ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder 0 trials
  • Aase-Smith syndrome 0 trials
  • Al Gazali Khidr Prem Chandran syndrome 0 trials
  • B4GALT1-congenital disorder of glycosylation 0 trials
  • Bailey-Bloch congenital myopathy 0 trials
  • Bardet-Biedl syndrome 11 0 trials
  • CTCF-related neurodevelopmental disorder 0 trials
  • DYRK1A-related intellectual disability syndrome 0 trials Sub-types →
  • EEM syndrome 0 trials
  • Houge-Janssens syndrome 1 0 trials
  • Johanson-Blizzard syndrome 0 trials
  • MYH7-related skeletal myopathy 0 trials
  • Myhre syndrome 0 trials
  • PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome 0 trials
  • Pierpont syndrome 0 trials
  • Pitt-Hopkins-like syndrome 2 0 trials
  • Prader-Willi-like syndrome 0 trials Sub-types →
  • Ritscher-Schinzel syndrome 0 trials Sub-types →
  • SIN3A-related intellectual disability syndrome 0 trials Sub-types →
  • SLC39A8-CDG 0 trials
  • Schinzel-Giedion syndrome 0 trials
  • TELO2-related intellectual disability-neurodevelopmental disorder 0 trials
  • Wieacker-Wolff syndrome 0 trials
  • X-linked adrenal hypoplasia congenita 0 trials Sub-types →
  • X-linked congenital stationary night blindness 0 trials Sub-types →
  • X-linked intellectual disability with marfanoid habitus 0 trials
  • X-linked intellectual disability, Cabezas type 0 trials
  • X-linked intellectual disability, Pai type 0 trials
  • X-linked intellectual disability, Stevenson type 0 trials
  • X-linked intellectual disability, Stoll type 0 trials
  • X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome 0 trials
  • X-linked intellectual disability-cubitus valgus-dysmorphism syndrome 0 trials
  • X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome 0 trials
  • X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome 0 trials
  • X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome 0 trials
  • X-linked intellectual disability-plagiocephaly syndrome 0 trials
  • X-linked intellectual disability-short stature-overweight syndrome 0 trials
  • X-linked recessive mitochondrial myopathy 0 trials
  • Adult-onset nemaline myopathy 0 trials
  • Alpha-actinopathy 0 trials Sub-types →
  • Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome 0 trials
  • Autosomal dominant primary microcephaly 0 trials Sub-types →
  • Autosomal recessive spinocerebellar ataxia 20 0 trials
  • Blepharophimosis - intellectual disability syndrome, MKB type 0 trials
  • Cardiac anomalies - developmental delay - facial dysmorphism syndrome 0 trials
  • Cerebellar-facial-dental syndrome 0 trials
  • Cone-rod synaptic disorder, congenital nonprogressive 0 trials
  • Congenital abducens nerve palsy 0 trials
  • Congenital achiasma 0 trials
  • Congenital axonal neuropathy with encephalopathy 0 trials
  • Congenital cataracts-facial dysmorphism-neuropathy syndrome 0 trials
  • Congenital epulis 0 trials
  • Congenital fibrosis of extraocular muscles type 1 0 trials
  • Congenital insensitivity to pain with hyperhidrosis 0 trials
  • Congenital insensitivity to pain with severe intellectual disability 0 trials
  • Congenital insensitivity to pain-hypohidrosis syndrome 0 trials
  • Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome 0 trials
  • Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type 0 trials
  • Congenital myasthenic syndrome 15 0 trials
  • Congenital myasthenic syndrome 18 0 trials
  • Congenital myasthenic syndrome 6 0 trials
  • Congenital myasthenic syndrome with tubular aggregates 0 trials Sub-types →
  • Congenital myopathy 7A, myosin storage, autosomal dominant 0 trials
  • Congenital neuronal ceroid lipofuscinosis 10 0 trials
  • Congenital oculomotor nerve palsy 0 trials
  • Congenital or early infantile CACH syndrome 0 trials
  • Congenital retinal arteriovenous communication 0 trials
  • Congenital stationary night blindness 1B 0 trials
  • Congenital stationary night blindness 1D 0 trials
  • Congenital stationary night blindness 1G 0 trials
  • Congenital stationary night blindness autosomal dominant 3 0 trials
  • Congenital trigeminal anesthesia 0 trials
  • Craniorachischisis 0 trials
  • Developmental and epileptic encephalopathy, 15 0 trials
  • Developmental and epileptic encephalopathy, 18 0 trials
  • Developmental and epileptic encephalopathy, 23 0 trials
  • Developmental and epileptic encephalopathy, 36 0 trials
  • Developmental and epileptic encephalopathy, 50 0 trials
  • Developmental and epileptic encephalopathy, 73 0 trials
  • Developmental and epileptic encephalopathy, 77 0 trials
  • Developmental malformations-deafness-dystonia syndrome 0 trials
  • Diastematomyelia 0 trials
  • Distal arthrogryposis Moore weaver type 0 trials
  • Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome 0 trials
  • Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome 0 trials
  • Familial congenital palsy of trochlear nerve 0 trials
  • Fibrosis of extraocular muscles, congenital, 2 0 trials
  • Fibrosis of extraocular muscles, congenital, 3c 0 trials
  • Fibrosis of extraocular muscles, congenital, 5 0 trials
  • Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome 0 trials
  • Holoprosencephaly 0 trials Sub-types →
  • Holoprosencephaly-hypokinesia-congenital contractures syndrome 0 trials
  • Hyaline body myopathy 0 trials
  • Hypomyelinating leukodystrophy 10 0 trials
  • Hypotonia, infantile, with psychomotor retardation and characteristic facies 0 trials Sub-types →
  • Infantile-onset X-linked spinal muscular atrophy 0 trials
  • Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies 0 trials
  • Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold 0 trials
  • Intellectual disability, Buenos-Aires type 0 trials
  • Intellectual disability, Wolff type 0 trials
  • Intellectual disability, X-linked, syndromic 33 0 trials
  • Intellectual disability, autosomal dominant 47 0 trials
  • Intellectual disability, autosomal dominant 48 0 trials
  • Intellectual disability, autosomal recessive 12 0 trials
  • Intellectual disability, autosomal recessive 53 0 trials
  • Intellectual disability-sparse hair-brachydactyly syndrome 0 trials
  • Intermediate nemaline myopathy 0 trials Sub-types →
  • Isolated exencephaly 0 trials
  • Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome 0 trials
  • Lissencephaly spectrum disorders 0 trials Sub-types →
  • Macrocephaly-short stature-paraplegia syndrome 0 trials
  • Macrocephaly-spastic paraplegia-dysmorphism syndrome 0 trials
  • Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome 0 trials
  • Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome 0 trials
  • Multiple congenital anomalies-hypotonia-seizures syndrome 2 0 trials
  • Multiple pterygium-malignant hyperthermia syndrome 0 trials
  • Myasthenia, congenital, refractory to acetylcholinesterase inhibitors 0 trials
  • Myasthenic syndrome, congenital, 22 0 trials
  • Myasthenic syndrome, congenital, 23, presynaptic 0 trials
  • Myasthenic syndrome, congenital, 24, presynaptic 0 trials
  • Myasthenic syndrome, congenital, 25, presynaptic 0 trials
  • Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive 0 trials
  • Myofibrillar myopathy 1 0 trials
  • Myofibrillar myopathy 3 0 trials
  • Myofibrillar myopathy 4 0 trials
  • Myofibrillar myopathy 5 0 trials
  • Myofibrillar myopathy 7 0 trials Sub-types →
  • Myopathy, myofibrillar, 13, with rimmed vacuoles 0 trials
  • Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies 0 trials
  • Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome 0 trials Sub-types →
  • Night blindness, congenital stationary, type1i 0 trials
  • Periventricular nodular heterotopia 0 trials Sub-types →
  • Prenatal-onset spinal muscular atrophy with congenital bone fractures 0 trials Sub-types →
  • Progressive myoclonic epilepsy type 3 0 trials
  • Radioulnar synostosis-developmental delay-hypotonia syndrome 0 trials
  • Schizencephaly 0 trials Sub-types →
  • Segmental spinal dysgenesis 0 trials
  • Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome 0 trials
  • Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome 0 trials
  • Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome 0 trials
  • Short stature-brachydactyly-obesity-global developmental delay syndrome 0 trials
  • Spastic paraplegia-severe developmental delay-epilepsy syndrome 0 trials
  • Spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis 0 trials
  • Subcortical band heterotopia 0 trials Sub-types →
  • Syndromic X-linked intellectual disability 34 0 trials
  • Syndromic X-linked intellectual disability 7 0 trials
  • Syndromic X-linked intellectual disability Abidi type 0 trials
  • Syndromic X-linked intellectual disability Claes-Jensen type 0 trials
  • Syndromic X-linked intellectual disability Shashi type 0 trials
  • Syndromic X-linked intellectual disability Siderius type 0 trials
  • Typical nemaline myopathy 0 trials Sub-types →
• Infectious disorder of the nervous system 4 trials · 232 incl. sub-types
  10 sub-types

  • Central nervous system infectious disorder 10 trials · 163 incl. sub-types Sub-types →
  • Tetanus 44 trials Sub-types →
  • Rabies 27 trials
  • Tropical spastic paraparesis 3 trials
  • Cytomegalovirus retinitis 2 trials
  • Tabes dorsalis 2 trials
  • Histoplasmosis retinitis 1 trial
  • Ophthalmic herpes zoster 0 trials
  • Postinfectious cerebellitis 0 trials
  • Tick paralysis 0 trials
• Neurocutaneous syndrome 2 trials · 171 incl. sub-types
  9 sub-types

  • Neurofibromatosis 19 trials · 94 incl. sub-types Sub-types →
  • Tuberous sclerosis 41 trials · 44 incl. sub-types Sub-types →
  • Von Hippel-Lindau disease 27 trials
  • Sturge-Weber syndrome 8 trials
  • Nevoid basal cell carcinoma syndrome 5 trials Sub-types →
  • Neurocutaneous melanocytosis 1 trial
  • Wyburn-Mason syndrome 0 trials
  • Phakomatosis pigmentokeratotica 0 trials
  • Phakomatosis pigmentovascularis 0 trials Sub-types →
• Atactic disorder 5 trials · 148 incl. sub-types
  4 sub-types

  • Cerebellar ataxia 40 trials · 144 incl. sub-types Sub-types →
  • Hereditary ataxia 2 trials · 119 incl. sub-types Sub-types →
  • Acquired ataxia 0 trials · 1 incl. sub-types Sub-types →
  • Sensory ataxia 0 trials Sub-types →
• AL amyloidosis 93 trials · 99 incl. sub-types
  2 sub-types

  • Primary systemic amyloidosis 22 trials
  • Primary localized amyloidosis 0 trials
• Neuromyelitis optica 85 trials
  3 sub-types

  • Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies 5 trials
  • Neuromyelitis optica spectrum disorder with anti-MOG antibodies 0 trials
  • Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies 0 trials
• Primary orthostatic hypotension 12 trials · 83 incl. sub-types
  2 sub-types

  • Inherited orthostatic hypotension 0 trials · 71 incl. sub-types Sub-types →
  • Peripheral motor neuropathy-dysautonomia syndrome 0 trials
• Developmental disability 82 trials
  5 sub-types

  • Chitty Hall Webb syndrome 0 trials
  • Bagatelle Cassidy syndrome 0 trials
  • Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome 0 trials
  • Psychosocial short stature 0 trials
  • Radioulnar synostosis-developmental delay-hypotonia syndrome 0 trials
• Toxic encephalopathy 28 trials · 75 incl. sub-types
  5 sub-types

  • Hepatic encephalopathy 45 trials Sub-types →
  • Carbon monoxide-induced delayed encephalopathy 1 trial
  • Manganese poisoning 1 trial
  • Minamata disease 0 trials
  • Chronic bilirubin encephalopathy 0 trials
• Specific learning disability 19 trials · 66 incl. sub-types
  2 sub-types

  • Specific language disorder 8 trials · 45 incl. sub-types Sub-types →
  • Non-verbal learning disability 2 trials
• Central nervous system malformation 5 trials · 51 incl. sub-types
  54 sub-types

  • Neural tube defect 12 trials · 23 incl. sub-types Sub-types →
  • Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes 0 trials · 10 incl. sub-types Sub-types →
  • Hoyeraal-Hreidarsson syndrome 3 trials
  • Pontocerebellar hypoplasia 1 trial · 3 incl. sub-types Sub-types →
  • Lhermitte-Duclos disease 2 trials
  • PHACE syndrome 2 trials
  • Joubert syndrome with oculorenal defect 1 trial Sub-types →
  • Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 1 trial
  • Cystic malformation of the posterior fossa 0 trials · 1 incl. sub-types Sub-types →
  • Syndromic X-linked intellectual disability 5 1 trial
  • Aase-Smith syndrome 0 trials
  • B4GALT1-congenital disorder of glycosylation 0 trials
  • Dandy-Walker malformation-postaxial polydactyly syndrome 0 trials
  • Gomez-Lopez-Hernandez syndrome 0 trials
  • Joubert syndrome with ocular defect 0 trials Sub-types →
  • NPHP3-related Meckel-like syndrome 0 trials
  • Ritscher-Schinzel syndrome 0 trials Sub-types →
  • SLC39A8-CDG 0 trials
  • TELO2-related intellectual disability-neurodevelopmental disorder 0 trials
  • X-linked cerebral-cerebellar-coloboma syndrome syndrome 0 trials
  • X-linked intellectual disability-cerebellar hypoplasia syndrome 0 trials
  • X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome 0 trials
  • Aprosencephaly cerebellar dysgenesis 0 trials
  • Arachnoid cyst 0 trials Sub-types →
  • Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome 0 trials
  • Autosomal recessive spinocerebellar ataxia 20 0 trials
  • Cerebellar-facial-dental syndrome 0 trials
  • Cerebral gigantism-jaw cysts syndrome 0 trials
  • Cervical hypertrichosis-peripheral neuropathy syndrome 0 trials
  • Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome 0 trials
  • Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome 0 trials
  • Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome 0 trials
  • Glioependymal/ependymal cyst 0 trials
  • Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome 0 trials
  • Hereditary cerebral malformation 0 trials
  • Holoprosencephaly-caudal dysgenesis syndrome 0 trials
  • Holoprosencephaly-hypokinesia-congenital contractures syndrome 0 trials
  • Hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism 0 trials
  • Isolated arhinencephaly 0 trials
  • Isolated bilateral hemispheric cerebellar hypoplasia 0 trials
  • Isolated cerebellar vermis agenesis 0 trials Sub-types →
  • Isolated cerebellar vermis hypoplasia 0 trials
  • Isolated unilateral hemispheric cerebellar hypoplasia 0 trials
  • Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome 0 trials
  • Macrocephaly-short stature-paraplegia syndrome 0 trials
  • Orofaciodigital syndrome type 6 0 trials
  • Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome 0 trials
  • Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome 0 trials
  • Pontine tegmental cap dysplasia 0 trials
  • Rhombencephalosynapsis 0 trials
  • Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome 0 trials
  • Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome 0 trials
  • Syndromic X-linked intellectual disability Najm type 0 trials
  • Tubulinopathy-associated dysgyria 0 trials
• Restless legs syndrome 45 trials
• Neuroendocrine disorder 0 trials · 42 incl. sub-types
  4 sub-types

  • Pineal body neoplasm 4 trials · 22 incl. sub-types Sub-types →
  • Central diabetes insipidus 5 trials · 12 incl. sub-types Sub-types →
  • Cyclic vomiting syndrome 8 trials
  • Posterior pituitary gland neoplasm 0 trials Sub-types →
• Qualitative or quantitative protein defects in neuromuscular diseases 0 trials · 30 incl. sub-types
  19 sub-types

  • Sarcoglycanopathy 3 trials · 10 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan 0 trials · 8 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of dystrophin 4 trials · 5 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of titin 0 trials · 4 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of tropomyosin 0 trials · 4 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of dysferlin 0 trials · 3 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of alpha-actin 0 trials · 2 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of nebulin 0 trials · 2 incl. sub-types Sub-types →
  • Collagen 6-related myopathy 1 trial Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of myofibrillar proteins 0 trials · 1 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of plectin 0 trials · 1 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of selenoprotein N1 0 trials · 1 incl. sub-types Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of telethonin 0 trials · 1 incl. sub-types Sub-types →
  • Alpha-actinopathy 0 trials Sub-types →
  • Caveolinopathy 0 trials Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of TRIM32 0 trials Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7) 0 trials Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of perlecan 0 trials Sub-types →
  • Neuromuscular disease caused by qualitative or quantitative defects of protein SERCA1 0 trials Sub-types →
• Neuronitis 20 trials
• Paraneoplastic neurologic syndrome 1 trial · 15 incl. sub-types
  7 sub-types

  • POEMS syndrome 8 trials
  • Lambert-Eaton myasthenic syndrome 4 trials
  • Opsoclonus-myoclonus syndrome 2 trials
  • Paraneoplastic cerebellar degeneration 1 trial
  • Cancer-associated retinopathy 0 trials
  • Paraneoplastic limbic encephalitis 0 trials Sub-types →
  • Paraneoplastic polyneuropathy 0 trials
• Stiff-person syndrome 12 trials
  3 sub-types

  • Classic stiff person syndrome 0 trials
  • Focal stiff limb syndrome 0 trials
  • Progressive encephalomyelitis with rigidity and myoclonus 0 trials
• Locked-in syndrome 11 trials
• Exercise-induced malignant hyperthermia 9 trials
• Persistent idiopathic facial pain 9 trials
• Synaptopathy 0 trials · 7 incl. sub-types
  1 sub-type

  • Neuromuscular junction disease 1 trial · 7 incl. sub-types Sub-types →
• Serotonin syndrome 6 trials
• Barre-Lieou syndrome 3 trials
• AA amyloidosis 2 trials
• Balint syndrome 2 trials
• Drug-induced akathisia 2 trials
• Drug-induced dyskinesia 2 trials
• Neurosarcoidosis 2 trials
  1 sub-type

  • Cerebral sarcoidosis 1 trial
• Sensory ganglionopathy 2 trials
  4 sub-types

  • Paraneoplastic sensory ganglionopathy 1 trial
  • Gasserian ganglion meningioma 0 trials
  • Geniculate ganglionitis 0 trials
  • Non-paraneoplastic sensory ganglionopathy 0 trials
• Dopa-responsive dystonia 1 trial · 2 incl. sub-types
  4 sub-types

  • TH-deficient dopa-responsive dystonia 1 trial
  • Dopa-responsive dystonia due to sepiapterin reductase deficiency 1 trial
  • Autosomal dominant dopa-responsive dystonia 0 trials Sub-types →
  • Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive 0 trials
• Periodic paralysis 1 trial · 2 incl. sub-types
  1 sub-type

  • Familial periodic paralysis 0 trials · 1 incl. sub-types Sub-types →
• Wallerian degeneration 1 trial
• Diplegia of upper limb 1 trial
• Neuroleptic malignant syndrome 1 trial
• Prepubertal anorexia nervosa 1 trial
• Radiculitis 1 trial
• Gerstmann syndrome 0 trials
• KIF1A related neurological disorder 0 trials
  3 sub-types

  • Hereditary spastic paraplegia 30 0 trials Sub-types →
  • Intellectual disability, autosomal dominant 9 0 trials
  • Neuropathy, hereditary sensory, type 2C 0 trials
• Sydenham chorea 0 trials
• Worster-Drought syndrome 0 trials
• Cerebellar hypoplasia-tapetoretinal degeneration syndrome 0 trials
• Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids 0 trials
• Corneal-cerebellar syndrome 0 trials
• Duplication of the pituitary gland 0 trials
• Hypothalamic adipsic hypernatraemia syndrome 0 trials
• Idiopathic recurrent stupor 0 trials
• Meningitis-retention syndrome 0 trials
• Neonatal brainstem dysfunction 0 trials
• Pachygyria-intellectual disability-epilepsy syndrome 0 trials
• Perineural cyst 0 trials
• Porencephaly-cerebellar hypoplasia-internal malformations syndrome 0 trials
• Post 5-alpha-reductase inhibitors treatment syndrome 0 trials
• Post-selective serotonin reuptake inhibitor sexual dysfunction 0 trials
• Rippling muscle disease with myasthenia gravis 0 trials
• Spontaneous periodic hypothermia 0 trials
• Symmetrical thalamic calcifications 0 trials
• Tubulinopathy 0 trials
  4 sub-types

  • TUBB3-related tubulinopathy 0 trials Sub-types →
  • Uner Tan Syndrome 0 trials
  • Complex cortical dysplasia with other brain malformations 5 0 trials
  • Tubulinopathy-associated dysgyria 0 trials
• Wet beriberi 0 trials