Neurological disorders

Coding system: SNOMED CT
Coding system release: unknown
Organisation: Office for National Statistics
Codelist ID: ons/neurological-disorders
Version ID: 54fabb61

Versions

No metadata has been provided for this codelist.

Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.

We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.

code	term
10394003	Friedreich's ataxia
1089411000000104	Cerebral infarction due to occlusion of cerebral artery
1089421000000105	Cerebral infarction due to stenosis of cerebral artery
110270004	Sequela of infection caused by Human poliovirus
111297002	Nonparalytic stroke
111501005	Congenital hereditary muscular dystrophy
111502003	Fukuyama congenital muscular dystrophy
111503008	Merosin deficient congenital muscular dystrophy
111504002	Walker-Warburg congenital muscular dystrophy
111505001	Muscle-eye-brain disease, congenital muscular dystrophy
111508004	Emery-Dreifuss muscular dystrophy
116288000	Paralytic stroke
116401000119105	Recurrent complex partial epilepsy
1212005	Childhood type dermatomyositis
124122005	Deficiency of 3-hydroxyacyl-CoA dehydrogenase
124166007	Deficiency of butyryl-CoA dehydrogenase
124621004	Deficiency of enoyl-coenzyme A hydratase
125081000119106	Cerebral infarction due to occlusion of precerebral artery
128212001	Spinal muscular atrophy, type II
128213006	Neuromuscular junction disorder
128596003	Medium-chain acyl-coenzyme A dehydrogenase deficiency
13973009	Grand mal status
140921000119102	Ischemic stroke without coma
14289006	Myopathy in hypopituitarism
14309005	Anterior choroidal artery syndrome
14637005	Late-infantile neuronal ceroid lipofuscinosis
15258001	Subclavian steal syndrome
15978431000119106	Thrombosis of right vertebral artery
16000351000119109	Cerebrovascular accident due to occlusion of left posterior cerebral artery
16000391000119104	Cerebrovascular accident due to occlusion of right posterior cerebral artery
16000431000119109	Cerebrovascular accident due to occlusion of right middle cerebral artery
16000511000119103	Cerebrovascular accident due to occlusion of left middle cerebral artery
16002031000119102	Cerebrovascular accident due to thrombus of right middle cerebral artery
16002111000119106	Cerebrovascular accident due to thrombus of left middle cerebral artery
16218291000119100	Acute cerebral ischemia
16371781000119100	Cerebellar stroke
16851005	Mitochondrial myopathy
16873003	Musicogenic seizure
186476008	Acute paralytic non-bulbar poliomyelitis
186478009	Acute paralytic poliomyelitis, vaccine-associated
186479001	Acute paralytic poliomyelitis, wild virus, imported
186480003	Acute paralytic poliomyelitis, wild virus, indigenous
189198006	Epileptic drop attack
191382009	Chronic congestive splenomegaly
191397007	Pseudocholinesterase deficiency
192686004	Polioencephalitis
192845009	Myoclonic encephalopathy
192979009	Generalized non-convulsive epilepsy
192981006	Epileptic seizures - atonic
192982004	Epileptic seizures - akinetic
192991000	Epileptic seizures - clonic
192992007	Epileptic seizures - myoclonic
192993002	Epileptic seizures - tonic
192999003	Partial epilepsy with impairment of consciousness
193000002	Temporal lobe epilepsy
193002005	Psychosensory epilepsy
193003000	Mesiobasal limbic epilepsy
193004006	Epileptic automatism
193008009	Somatosensory epilepsy
193009001	Partial epilepsy with autonomic symptoms
193010006	Visual reflex epilepsy
193011005	Unilateral epilepsy
193021002	Cursive (running) epilepsy
193022009	Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset
193206003	Persistent neonatal myasthenia gravis
193207007	Juvenile or adult myasthenia gravis
193209005	Myasthenic syndrome due to another disorder
193212008	Myasthenic syndrome due to hypothyroidism
193213003	Myasthenic syndrome due to pernicious anemia
193214009	Myasthenic syndrome due to thyrotoxicosis
193216006	Congenital and developmental myasthenia
193225000	Hereditary progressive muscular dystrophy
193227008	Pelvic muscular dystrophy
193230001	Distal muscular dystrophy with juvenile onset
193237003	Myotonic disorder
193238008	Infantile myotonia
193246009	Symptomatic inflammatory myopathy associated with another disorder
193248005	Myopathy due to disseminated lupus erythematosus
193249002	Myopathy due to polyarteritis nodosa
193250002	Myopathy due to rheumatoid arthritis
193251003	Sarcoid myopathy
193252005	Myopathy due to scleroderma
193253000	Myopathy due to Sjögren's disease
195163003	Intracerebral hemorrhage (& [cerebrovascular accident due to])
195165005	Basal ganglia hemorrhage
195167002	External capsule hemorrhage
195169004	Intracerebral hemorrhage, multiple localized
195185009	Cerebral infarct due to thrombosis of precerebral arteries
195186005	Cerebral infarction due to embolism of precerebral arteries
195189003	Cerebral infarction due to thrombosis of cerebral arteries
195190007	Cerebral infarction due to embolism of cerebral arteries
195200006	Carotid artery syndrome hemispheric
195201005	Multiple and bilateral precerebral artery syndromes
195206000	Intermittent cerebral ischemia
195209007	Middle cerebral artery syndrome
195210002	Anterior cerebral artery syndrome
195211003	Posterior cerebral artery syndrome
195212005	Brainstem stroke syndrome
195213000	Cerebellar stroke syndrome
195216008	Left sided cerebral hemisphere cerebrovascular accident
195217004	Right sided cerebral hemisphere cerebrovascular accident
195230003	Cerebral infarction due to cerebral venous thrombosis, non-pyogenic
19598007	Generalized epilepsy
196136009	Lung disease co-occurrent with polymyositis
199451000000106	Simple partial epileptic seizure
19972008	Postencephalitic parkinsonism
20059004	Occlusion of cerebral artery
20908003	Subcortical cerebral hemorrhage
21764004	Renal carnitine transport defect
22062008	X-linked glutaric aciduria, type 2
22886006	Glutaric aciduria, type 2
230191005	Rasmussen syndrome
230237004	Progressive spinocerebellar ataxia with decreased tendon reflexes
230238009	Progressive spinocerebellar ataxia with retained tendon reflexes
230246005	Progressive bulbar palsy of childhood
230247001	Distal spinal muscular atrophy
230248006	Scapuloperoneal spinal muscular atrophy
230249003	Facioscapulohumeral spinal muscular atrophy
230250003	Facioscapulohumeral spinal muscular atrophy with sensory loss
230251004	Scapulohumeral spinal muscular atrophy
230252006	Oculopharyngeal spinal muscular atrophy
230253001	Bulbospinal neuronopathy
230254007	Western Pacific motor neurone disease
230255008	Madras-type motor neurone disease
230257000	Paraneoplastic motor neurone disease
230258005	Amyotrophic lateral sclerosis with dementia
230264003	Troyer syndrome
230274000	Frontal lobe degeneration with motor neurone disease
230291001	Juvenile Parkinson's disease
230292008	Secondary parkinsonism
230296006	Vascular parkinsonism
230381009	Localization-related epilepsy
230387008	Benign occipital epilepsy of childhood - early onset variant
230389006	Primary inherited reading epilepsy
230390002	Localization-related symptomatic epilepsy
230391003	Amygdalo-hippocampal epilepsy
230392005	Rhinencephalic epilepsy
230393000	Lateral temporal epilepsy
230394006	Frontal lobe epilepsy
230395007	Supplementary motor epilepsy
230396008	Cingulate epilepsy
230397004	Anterior frontopolar epilepsy
230398009	Orbitofrontal epilepsy
230399001	Dorsolateral epilepsy
230400008	Opercular epilepsy
230401007	Non-progressive Kozhevnikow syndrome
230403005	Parietal lobe epilepsy
230404004	Occipital lobe epilepsy
230405003	Chronic progressive epilepsia partialis continua of childhood
230406002	Localization-related symptomatic epilepsy with specific precipitant
230407006	Hemiplegia-hemiconvulsion-epilepsy syndrome
230408001	Localization-related cryptogenic epilepsy
230415009	Cryptogenic generalized epilepsy
230416005	Cryptogenic West syndrome
230417001	Symptomatic West syndrome
230418006	Lennox-Gastaut syndrome
230419003	Cryptogenic Lennox-Gastaut syndrome
230420009	Symptomatic Lennox-Gastaut syndrome
230421008	Myoclonic astatic epilepsy
230422001	Myoclonic absence epilepsy
230423006	Unverricht-Lundborg syndrome
230425004	Lafora disease
230426003	Myoclonic epilepsy with ragged red fibers
230427007	Cryptogenic myoclonic epilepsy
230428002	Idiopathic myoclonic epilepsy
230429005	Early infantile epileptic encephalopathy with suppression bursts
230430000	Symptomatic myoclonic epilepsy
230435005	Epilepsy undetermined whether focal or generalized
230439004	Epilepsy with continuous spike wave during slow-wave sleep
230440002	Secondary reading epilepsy
230441003	Drug-induced epilepsy
230443000	Narcotic withdrawal epilepsy
230444006	Menstrual epilepsy
230445007	Nocturnal epilepsy
230447004	Eyelid myoclonus with absences
230448009	Writing epilepsy
230450001	Eating epilepsy
230452009	Toothbrushing epilepsy
230453004	Decision-making epilepsy
230454005	Aquagenic epilepsy
230455006	Self-induced non-photosensitive epilepsy
230456007	Status epilepticus
230457003	Non-convulsive status epilepticus with three per second spike wave
230458008	Non-convulsive status epilepticus without three per second spike wave
230459000	Non-convulsive simple partial status epilepticus
230460005	Complex partial status epilepticus
230669004	Genetically determined myasthenia
230670003	Familial infantile myasthenia
230671004	Acetylcholine resynthesis deficiency
230672006	Congenital myasthenic syndrome
230673001	Congenital end-plate acetylcholine receptor deficiency
230674007	Pseudomyopathic myasthenia
230675008	Slow channel syndrome
230676009	Putative defect in acetylcholine synthesis or packaging
230677000	Congenital end-plate acetylcholinesterase deficiency
230678005	Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency
230679002	Abnormality of synaptic vesicles
230682007	Penicillamine-induced myasthenia
230685009	Myasthenia gravis associated with thymoma
230686005	Generalized myasthenia
230687001	Myopathy in myasthenia gravis
230690007	Cerebrovascular accident
230691006	Cerebrovascular accident due to occlusion of cerebral artery
230692004	Infarction - precerebral
230693009	Anterior cerebral circulation infarction
230694003	Total anterior cerebral circulation infarction
230695002	Partial anterior cerebral circulation infarction
230696001	Posterior cerebral circulation infarction
230698000	Lacunar infarction
230699008	Pure motor lacunar infarction
230700009	Pure sensory lacunar infarction
230701008	Pure sensorimotor lacunar infarction
230702001	Lacunar ataxic hemiparesis
230703006	Dysarthria-clumsy hand syndrome
230704000	Multi-infarct state
230706003	Hemorrhagic cerebral infarction
230707007	Anterior cerebral circulation hemorrhagic infarction
230708002	Posterior cerebral circulation hemorrhagic infarction
230709005	Massive supratentorial cerebral hemorrhage
230710000	Lobar cerebral hemorrhage
230711001	Thalamic hemorrhage
230712008	Lacunar hemorrhage
230713003	Stroke of uncertain pathology
230714009	Anterior circulation stroke of uncertain pathology
230715005	Posterior circulation stroke of uncertain pathology
230716006	Carotid territory transient ischemic attack
230717002	Vertebrobasilar territory transient ischemic attack
230784003	Congenital pseudobulbar palsy
237997005	Very long chain acyl-coenzyme A dehydrogenase deficiency
237999008	Mitochondrial trifunctional protein deficiency
238001003	Carnitine palmitoyltransferase I deficiency
238002005	Carnitine palmitoyltransferase II deficiency
238003000	Carnitine acylcarnitine translocase deficiency
238026007	Infantile GM1 gangliosidosis
238936001	Sclerodermatomyositis
239898008	Polymyositis with malignant disease
239899000	Polymyositis associated with autoimmune disease
239901009	Dermatomyositis with malignant disease
240046001	Muscular dystrophy with predominantly proximal limb girdle distribution
240047005	X-linked muscular dystrophy with limb girdle distribution
240048000	X-linked muscular dystrophy with abnormal dystrophin
240049008	Intermediate X-linked muscular dystrophy
240050008	Manifesting female carrier of X-linked muscular dystrophy
240051007	X-linked limb girdle muscular dystrophy with normal dystrophin
240052000	Ji muscular dystrophy
240053005	Hereditary myopathy limited to females
240054004	Autosomal recessive muscular dystrophy with limb girdle distribution
240055003	Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
240056002	Severe autosomal recessive muscular dystrophy of childhood - North African type
240057006	Autosomal recessive muscular dystrophy with gene located at 15q
240058001	Reunion-Indiana Amish type muscular dystrophy
240059009	Congenital muscular dystrophy
240060004	Western type of congenital muscular dystrophy
240061000	Congenital muscular dystrophy with arthrogryposis multiplex congenita
240062007	Ullrich congenital muscular dystrophy
240063002	Eichsfeld type congenital muscular dystrophy
240064008	Hutterite type of muscular dystrophy
240065009	Adult onset autosomal recessive muscular dystrophy with normal dystrophin
240067001	Autosomal dominant muscular dystrophy with limb girdle distribution
240068006	Autosomal dominant muscular dystrophy with gene located at 5q31
240069003	Late onset proximal muscular dystrophy with dysarthria
240070002	Muscular dystrophy not predominantly limb girdle in distribution
240071003	X-linked muscular dystrophy not predominantly limb girdle
240072005	Benign scapuloperoneal muscular dystrophy with cardiomyopathy
240073000	Autosomal recessive muscular dystrophy not predominantly limb girdle
240074006	Scapulohumeral muscular dystrophy
240075007	Autosomal dominant muscular dystrophy not predominantly limb girdle
240076008	Benign scapuloperoneal muscular dystrophy
240077004	Severe scapuloperoneal muscular dystrophy with cardiomyopathy
240078009	Benign congenital muscular dystrophy with finger flexion contractures
240460008	Acute paralytic poliomyelitis
240630008	Hyperimmune malarious splenomegaly
241006	Epilepsia partialis continua
24654003	Weber-Gubler syndrome
249892007	Progressive pseudobulbar palsy
25133001	Completed stroke
25425008	Autosomal recessive glutaric aciduria, type 2
256321009	Disorder of neuromuscular transmission
26111005	Metabolic myopathy
266257000	Transient ischemic attack
267581004	Progressive myoclonic epilepsy
267592003	Motor cortex epilepsy
267604001	Myasthenic syndrome due to diabetic mellitus
274100004	Cerebral hemorrhage
275434003	Stroke in the puerperium
276219001	Occipital cerebral infarction
276220007	Foville syndrome
276221006	Millard-Gubler syndrome
276222004	Top of basilar syndrome
276722003	Intracerebellar and posterior fossa hemorrhage
277373000	Severe childhood autosomal recessive muscular dystrophy
28055006	West syndrome
281240008	Extension of cerebrovascular accident
281357005	Idiopathic polymyositis
281358000	Idiopathic dermatomyositis
290741000119102	Intractable idiopathic partial epilepsy
291511000119103	Spontaneous hemorrhage of deep cerebral hemisphere
291531000119108	Spontaneous hemorrhage of cerebral hemisphere
291541000119104	Spontaneous hemorrhage of brain stem
29570005	Leigh's disease
297138001	Embolus of circle of Willis
305719002	Neuromyotonia
307127004	Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency
307128009	Combined long chain hydroxyacyl-coenzyme A dehydrogenase deficiency
307130006	3-Ketoacyl-coenzyme A triolase deficiency
307356008	Motor epilepsy
307357004	Jacksonian, focal or motor epilepsy
307363008	Multiple lacunar infarcts
307766002	Left sided cerebral infarction
307767006	Right sided cerebral infarction
308128006	Right sided intracerebral hemorrhage, unspecified
31097004	Post poliomyelitis syndrome
313307000	Epileptic seizure
31384009	Polymyositis
31839002	Myasthenia gravis, adult form
322112361000132104	Epilepsy due to scarring of brain
329461000119102	Cerebrovascular accident due to occlusion of left cerebellar artery by embolus
329481000119106	Occlusion of right middle cerebral artery
329491000119109	Occlusion of left middle cerebral artery
329561000119101	Occlusion of right posterior cerebral artery
329571000119107	Occlusion of left posterior cerebral artery
329641000119104	Cerebrovascular accident due to thrombus of basilar artery
329651000119102	Cerebrovascular accident due to thrombus of right carotid artery
330791000119108	Cerebrovascular accident due to thrombus of left carotid artery
34253008	Myopathy in Addison's disease
34781003	Vertebral artery syndrome
352818000	Tonic-clonic epilepsy
361123003	Psychomotor epilepsy
361268000	Alcohol-induced epilepsy
371040005	Thrombotic stroke
371041009	Embolic stroke
37340000	Motor neuron disease
37356005	Myoclonic seizure
373606000	Occlusive stroke
384993003	Periventricular hemorrhagic venous infarct
387732009	Becker muscular dystrophy
396230008	Dermatomyositis
398432008	Bulbar weakness
399091004	Facioscapulohumeral muscular dystrophy
39912006	Hereditary spastic paraplegia
407675009	Complex partial epileptic seizure
40956001	Guillain-Barré syndrome
413101007	Stress-induced epilepsy
413102000	Infarction of basal ganglia
413758000	Cardioembolic stroke
41574007	Paramyotonia congenita
41713005	Benedikt's syndrome
419921000000105	[X]Dermatopolymyositis, unspecified
4223005	Parkinsonism caused by drug
426107000	Acute lacunar infarction
426814001	Transient cerebral ischemia due to atrial fibrillation
426983002	Infarction of medulla oblongata
432504007	Cerebral infarction
434541000124109	Benign childhood epilepsy with centrotemporal spikes, refractory
434551000124106	Benign childhood epilepsy with centrotemporal spikes, non-refractory
44395000	Spastic tetraplegia with rigidity syndrome
44423001	Early myoclonic encephalopathy
444657001	Superior cerebellar artery syndrome
46251005	Corticospinal motor disease
48794007	Human immunodeficiency virus infection with infectious mononucleosis-like syndrome
49049000	Parkinson's disease
49422009	Cortical hemorrhage
49793008	Hereditary motor neuron disease
509341000000107	Petit-mal epilepsy
50967008	Gangliosidosis
51615001	Fibrosis of lung
52201006	Internal capsule hemorrhage
5262007	Spinal muscular atrophy
53509000	Myopathy in Cushing's disease
54280009	Kugelberg-Welander disease
54304004	Progressive bulbar palsy
55016009	Congenital muscular hypertrophy-cerebral syndrome
55051001	Myasthenia gravis, juvenile form
56267009	Multi-infarct dementia
56989000	Eaton-Lambert syndrome
57938005	Congenital myotonia, autosomal dominant form
57958006	Endocrine myopathy
57981008	Progressing stroke
58756001	Huntington's chorea
58795000	Distal muscular dystrophy
60738003	Secondary myopathy
62009002	Adult neuronal ceroid lipofuscinosis
63135006	Amyotonia congenita
64009001	Basilar artery syndrome
64383006	Werdnig-Hoffmann disease
64764001	Acute paralytic poliomyelitis, bulbar
65120008	Generalized convulsive epilepsy
67747009	Ocular muscular dystrophy
67992007	Multiple AND bilateral precerebral artery obstruction
68437005	Thyrotoxic myopathy
68618008	Rett's disorder
699866005	Progressive bulbar palsy with sensorineural deafness
702343002	Early onset myopathy with fatal cardiomyopathy
702373006	Hereditary myopathy with early respiratory failure
702383005	Distal myopathy 2
7033004	Petit mal status
703524005	Spinal muscular atrophy with progressive myoclonic epilepsy
711406009	Autosomal recessive axonal neuropathy with neuromyotonia
711483003	Spinal muscular atrophy with respiratory distress type 1
713275003	Splenomegaly co-occurrent with human immunodeficiency virus infection
71444005	Cerebral arterial thrombosis
715429006	Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
715565004	Lethal arthrogryposis co-occurrent with anterior horn cell disease
716278005	Jeavons syndrome
716722005	Acute motor sensory axonal Guillain-Barré syndrome
716723000	Guillain-Barré syndrome acute inflammatory demyelinating polyradiculoneuropathic form
717964007	Juvenile primary lateral sclerosis
718177001	Autosomal recessive limb girdle muscular dystrophy type 2F
71831005	Symptomatic generalized epilepsy
718555006	Juvenile amyotrophic lateral sclerosis
718572004	Bethlem myopathy
719836007	X-linked distal arthrogryposis multiplex congenita
722987009	Amyotrophic lateral sclerosis plus syndrome
723308003	Epidermolysis bullosa simplex with muscular dystrophy
723612001	Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
724429004	Stroke co-occurrent with migraine
725046003	Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9
725163002	X-linked spasticity, intellectual disability, epilepsy syndrome
725420009	Congenital muscular dystrophy Paradas type
726021008	Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
73192008	Multiple AND bilateral precerebral artery stenosis
732923001	Hemorrhage of medulla oblongata
73297009	Muscular dystrophy
733490006	Distal myopathy with early respiratory muscle involvement
734383005	Thrombosis of left middle cerebral artery
734384004	Thrombosis of right middle cerebral artery
734434007	Pyridoxine-dependent epilepsy
734961002	Embolus of left posterior cerebral artery
734963004	Embolus of right posterior cerebral artery
734964005	Embolus of left middle cerebral artery
734965006	Embolus of right middle cerebral artery
7379000	Pseudobulbar palsy
75023009	Post-traumatic epilepsy
75038005	Cerebellar hemorrhage
75072002	Nemaline myopathy
75543006	Cerebral embolism
762629007	Occlusion of right middle cerebral artery by embolus
762630002	Occlusion of left middle cerebral artery by embolus
762651004	Occlusion of right posterior cerebral artery by embolus
762652006	Occlusion of left posterior cerebral artery by embolus
763067000	Autosomal dominant congenital benign spinal muscular atrophy
763314009	Congenital muscular dystrophy with hyperlaxity
763349002	Progressive myoclonic epilepsy with dystonia
763533003	Distal hereditary motor neuropathy Jerash type
763534009	Hot water reflex epilepsy
763622006	Thinking epilepsy
763632004	Startle epilepsy
763802009	Micturition induced epilepsy
763827002	Orgasm induced epilepsy
763829004	Oculopharyngodistal myopathy
764522009	Familial focal epilepsy with variable foci
764812008	Autosomal recessive myogenic arthrogryposis multiplex congenita
764944006	Congenital muscular dystrophy type 1B
765089003	Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome
765093009	Rolandic epilepsy, speech dyspraxia syndrome
765170001	Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy
765197008	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
765216006	Audiogenic epilepsy
76670001	Duchenne muscular dystrophy
766764008	X-linked distal spinal muscular atrophy type 3
766815007	Perioral myoclonia with absences
766932005	Hypothalamic hamartoma with gelastic seizure
768666006	Syntaxin binding protein 1 encephalopathy with epilepsy
7689009	Reading seizure
770405003	Benign familial mesial temporal lobe epilepsy
770431001	Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation
770558006	Late-onset distal myopathy Markesbery Griggs type
770560008	Lissencephaly due to LIS1 mutation
770596007	Rippling muscle disease with myasthenia gravis
770622009	Benign infantile focal epilepsy with midline spikes and waves during sleep
770623004	Benign occipital lobe epilepsy
770624005	Benign partial epilepsy of infancy with complex partial seizures
770627003	Desmin-related myofibrillar myopathy
770643005	Mesial temporal lobe epilepsy with hippocampal sclerosis
770722002	Proximal myopathy with extrapyramidal signs
770727008	Spinal muscular atrophy with respiratory distress type 2
770758009	New-onset refractory status epilepticus
770786001	Hereditary inclusion body myopathy type 4
770787005	Benign Samaritan congenital myopathy
770939009	Huntington disease-like 3
77097004	Oculopharyngeal muscular dystrophy
771141002	Benign partial epilepsy with secondarily generalized seizures in infancy
771142009	Cortical dysplasia with focal epilepsy syndrome
771144005	Hereditary motor and sensory neuropathy with acrodystrophy
771223000	Infantile epileptic dyskinetic encephalopathy
771238004	Spinal atrophy, ophthalmoplegia, pyramidal syndrome
771267003	Congenital muscular dystrophy with integrin alpha-7 deficiency
771272007	Congenital muscular dystrophy due to lamin A/C mutation
7713009	Intrapontine hemorrhage
771302009	Autosomal recessive lower motor neuron disease with childhood onset
771303004	Severe neonatal onset encephalopathy with microcephaly
771306007	Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome
771448004	Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency
771469002	Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
771475006	Young adult-onset distal hereditary motor neuropathy
772129007	Autosomal dominant childhood-onset proximal spinal muscular atrophy
773230003	Cyclin-dependent kinase-like 5 deficiency
773306002	Congenital lethal myopathy Compton North type
773421009	Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
773497001	Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome
773548008	Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome
773555005	Severe neurodegenerative syndrome with lipodystrophy
773643006	Multiple congenital anomalies, hypotonia, seizures syndrome type 2
773729007	X-linked myopathy with postural muscle atrophy
774148007	Polyglucosan body myopathy type 1
77461000119109	Myasthenia gravis with exacerbation
77471000119103	Myasthenia gravis without exacerbation
776087007	Autosomal recessive cerebral atrophy
778001003	Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy
778029000	FAST kinase domains 2-related infantile mitochondrial encephalomyopathy
778047006	Myoclonic epilepsy in non-progressive encephalopathy
778050009	Idiopathic eosinophilic myositis
778060000	Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy
778063003	Cryptogenic late-onset epileptic spasms
77956009	Steinert myotonic dystrophy syndrome
782737003	Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome
782743001	Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions
782744007	Lipoic acid synthetase deficiency
782772000	Congenital muscular dystrophy with intellectual disability and severe epilepsy
782883004	Fatal infantile hypertonic myofibrillar myopathy
783010003	Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome
783012006	Parkinsonian pyramidal syndrome
783055005	Progressive myoclonic epilepsy type 5
783062001	Progressive myoclonic epilepsy type 6
783064000	Progressive myoclonic epilepsy type 3
783139000	Progressive myoclonic epilepsy type 8
783174004	Congenital muscular dystrophy with intellectual disability
783175003	Congenital muscular dystrophy without intellectual disability
783176002	Congenital muscular dystrophy with cerebellar involvement
783734000	Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency
783739005	Familial temporal lobe epilepsy
784341001	Amyotrophic lateral sclerosis type 4
784342008	Familial infantile myoclonic epilepsy
784345005	Malignant migrating partial seizures of infancy
784371009	Huntington disease-like 1
784372002	Familial mesial temporal lobe epilepsy with febrile seizures
784377008	Autosomal dominant epilepsy with auditory features
78468005	Erb's muscular dystrophy
785298001	Muscle eye brain disease with bilateral multicystic leukodystrophy
785303004	Multiple congenital anomalies, hypotonia, seizures syndrome
78569004	Posterior inferior cerebellar artery syndrome
787037000	Congenital muscular dystrophy type 1A
788417006	Alopecia, epilepsy, intellectual disability syndrome Moynahan type
788880006	Cerebral ischemic stroke due to dissection of artery
788881005	Cerebral ischemic stroke due to aortic arch embolism
788882003	Cerebral ischemic stroke due to global hypoperfusion with watershed infarct
788883008	Cerebral ischemic stroke due to hypercoagulable state
789063000	Primary hyperaldosteronism, seizures, neurological abnormalities syndrome
79745005	Reflex epilepsy
80976008	Myasthenic crisis
81211007	Primary lateral sclerosis
82077006	Myotubular myopathy
84201000119105	Intractable partial temporal lobe epilepsy with impairment of consciousness
84590007	Lower motor neuron disease
84757009	Epilepsy
85505000	Adult spinal muscular atrophy
85672005	Anterior horn cell disease
86044005	Amyotrophic lateral sclerosis
860804005	Epilepsy due to infectious encephalitis
860806007	Epilepsy due to infectious meningitis
860815000	Epilepsy due to neonatal central nervous system infection
864471000000106	Anterior opercular syndrome
870288002	Parkinsonism caused by methanol
870295006	Parkinsonism caused by carbon disulfide
870544005	Occlusion of distal basilar artery
870579007	Occlusion of branch of basilar artery
87555007	Claude's syndrome
87694001	Pyruvate carboxylase deficiency
88923002	Progressive muscular atrophy
89525009	Gelastic seizure
90099008	Subcortical leukoencephalopathy
9105005	Muscle adenosine monophosphate deaminase deficiency
91637004	Myasthenia gravis
93153005	Limb-girdle muscular dystrophy
95208000	Photogenic epilepsy
95454007	Brain stem hemorrhage
95457000	Brain stem infarction
95460007	Cerebellar infarction
95647008	Upper motor neuron disease

Codes not in the full codelist are in faint grey.

Neurological disorders

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