Other Neurological Conditions (SNOMED)
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- unknown
-
Organisation
- OpenSAFELY
-
Codelist ID
- opensafely/other-neurological-conditions-snomed
-
Version Tag
- 2020-06-02
-
Version ID
- 371c5810
Versions
About
Description
Automatically-generated equivalent of Other Neurological Conditions
Methodology
See code on GitHub
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.
| id | name | active | notes |
|---|---|---|---|
| 230777006 | Monoplegic cerebral palsy affecting upper limb (disorder) | y | direct mapping |
| 230780007 | Dyskinetic cerebral palsy (disorder) | y | direct mapping |
| 907151000000108 | Seen by Parkinson's disease service (finding) | y | direct mapping |
| 193207007 | Juvenile or adult myasthenia gravis (disorder) | y | direct mapping |
| 448054001 | Adult onset autosomal dominant leukodystrophy (disorder) | y | direct mapping |
| 230301006 | Akinetic-rigid form of Huntington's disease (disorder) | y | direct mapping |
| 444024002 | Multiple system atrophy, cerebellar variant (disorder) | y | direct mapping |
| 230773005 | Spastic cerebral palsy (disorder) | y | direct mapping |
| 230686005 | Generalized myasthenia (disorder) | y | direct mapping |
| 193225000 | Hereditary progressive muscular dystrophy (disorder) | y | direct mapping |
| 1593000 | Infantile hemiplegia (disorder) | y | direct mapping |
| 425390006 | Dementia associated with Parkinson's Disease (disorder) | y | direct mapping |
| 307324001 | Spastic foot (finding) | y | direct mapping |
| 813921000000104 | Spastic hemiplegic cerebral palsy (disorder) | y | direct mapping |
| 367591000000101 | Management of multiple sclerosis in early disease phase (regime/therapy) | y | direct mapping |
| 792004 | Jakob-Creutzfeldt disease (disorder) | y | direct mapping |
| 438511000 | Benign multiple sclerosis (disorder) | y | direct mapping |
| 240054004 | Autosomal recessive muscular dystrophy with limb girdle distribution (disorder) | y | direct mapping |
| 192685000 | Subacute sclerosing panencephalitis (disorder) | y | direct mapping |
| 28978003 | Progressive supranuclear ophthalmoplegia (disorder) | y | direct mapping |
| 278284007 | Right hemiplegia (disorder) | y | direct mapping |
| 230669004 | Genetically determined myasthenia (disorder) | y | direct mapping |
| 367561000000107 | Management of multiple sclerosis in onset phase (regime/therapy) | y | direct mapping |
| 91637004 | Myasthenia gravis (disorder) | y | direct mapping |
| 58795000 | Distal muscular dystrophy (disorder) | y | direct mapping |
| 361273006 | Alcoholic cerebellar degeneration (disorder) | y | direct mapping |
| 399091004 | Facioscapulohumeral muscular dystrophy (disorder) | y | direct mapping |
| 904531000000100 | Bilateral spastic cerebral palsy (disorder) | y | direct mapping |
| 230291001 | Juvenile Parkinson's disease (disorder) | y | direct mapping |
| 230299004 | Juvenile onset Huntington's disease (disorder) | y | direct mapping |
| 75019001 | Athetoid cerebral palsy (disorder) | y | direct mapping |
| 56989000 | Eaton-Lambert syndrome (disorder) | y | direct mapping |
| 80935004 | Flaccid hemiplegia (disorder) | y | direct mapping |
| 230672006 | Congenital myasthenia (disorder) | y | direct mapping |
| 240064008 | Hutterite type of muscular dystrophy (disorder) | y | direct mapping |
| 230300007 | Late onset Huntington's disease (disorder) | y | direct mapping |
| 192818008 | Cerebral degeneration due to Creutzfeldt-Jakob disease (disorder) | y | direct mapping |
| 240063002 | Eichsfeld type congenital muscular dystrophy (disorder) | y | direct mapping |
| 278285008 | Left hemiplegia (disorder) | y | direct mapping |
| 193209005 | Myasthenic syndrome due to another disorder (disorder) | y | direct mapping |
| 307756005 | Cerebral palsy, not congenital or infantile, acute (disorder) | y | direct mapping |
| 361272001 | Cerebellar ataxia due to alcoholism (disorder) | y | direct mapping |
| 76670001 | Duchenne muscular dystrophy (disorder) | y | direct mapping |
| 24326000 | Metachromatic leukodystrophy, adult type (disorder) | y | direct mapping |
| 240058001 | Reunion-Indiana Amish type muscular dystrophy (disorder) | y | direct mapping |
| 240060004 | Western type of congenital muscular dystrophy (disorder) | y | direct mapping |
| 885831000000109 | Choreoathetoid cerebral palsy (disorder) | y | direct mapping |
| 192927008 | Multiple sclerosis of the spinal cord (disorder) | y | direct mapping |
| 240067001 | Autosomal dominant muscular dystrophy with limb girdle distribution (disorder) | y | direct mapping |
| 192958009 | Hypotonic cerebral palsy (disorder) | y | direct mapping |
| 387732009 | Becker muscular dystrophy (disorder) | y | direct mapping |
| 341551000000108 | Cerebral degeneration in Parkinson's disease (disorder) | y | direct mapping |
| 193206003 | Persistent neonatal myasthenia gravis (disorder) | y | direct mapping |
| 44359008 | Metachromatic leukodystrophy, juvenile type (disorder) | y | direct mapping |
| 24700007 | Multiple sclerosis (disorder) | y | direct mapping |
| 47683004 | Metachromatic leukodystrophy, late infantile type (disorder) | y | direct mapping |
| 240057006 | Autosomal recessive muscular dystrophy with gene located at 15q (disorder) | y | direct mapping |
| 515841000000104 | History of Parkinson's disease (situation) | y | direct mapping |
| 93153005 | Limb-girdle muscular dystrophy (disorder) | y | direct mapping |
| 111502003 | Fukuyama congenital muscular dystrophy (disorder) | y | direct mapping |
| 785851000000104 | Referral to community multiple sclerosis team (procedure) | y | direct mapping |
| 37340000 | Motor neuron disease (disorder) | y | direct mapping |
| 48721008 | Quadriplegic cerebral palsy (disorder) | y | direct mapping |
| 192926004 | Multiple sclerosis of the brainstem (disorder) | y | direct mapping |
| 277373000 | Severe childhood autosomal recessive muscular dystrophy (disorder) | y | direct mapping |
| 193230001 | Distal muscular dystrophy with juvenile onset (disorder) | y | direct mapping |
| 240052000 | Ji muscular dystrophy (disorder) | y | direct mapping |
| 425500002 | Secondary progressive multiple sclerosis (disorder) | y | direct mapping |
| 58193001 | Diplegic cerebral palsy (disorder) | y | direct mapping |
| 240076008 | Benign scapuloperoneal muscular dystrophy (disorder) | y | direct mapping |
| 128188000 | Cerebral palsy (disorder) | y | direct mapping |
| 230685009 | Myasthenia gravis associated with thymoma (disorder) | y | direct mapping |
| 205631000000104 | Multiple sclerosis multidisciplinary review (regime/therapy) | y | direct mapping |
| 439567002 | Malignant multiple sclerosis (disorder) | y | direct mapping |
| 230372003 | Acute relapsing multiple sclerosis (disorder) | y | direct mapping |
| 367681000000102 | Management of multiple sclerosis in palliative phase (regime/therapy) | y | direct mapping |
| 230254007 | Western Pacific motor neurone disease (disorder) | y | direct mapping |
| 111505001 | Muscle-eye-brain disease, congenital muscular dystrophy (disorder) | y | direct mapping |
| 10394003 | Friedreich's ataxia (disorder) | y | direct mapping |
| 759051000000102 | Multiple sclerosis monitoring first letter (procedure) | y | direct mapping |
| 758981000000100 | Multiple sclerosis monitoring administration (record artifact) | y | direct mapping |
| 240048000 | X-linked muscular dystrophy with abnormal dystrophin (disorder) | y | direct mapping |
| 54304004 | Progressive bulbar palsy (disorder) | y | direct mapping |
| 193216006 | Congenital and developmental myasthenia (disorder) | y | direct mapping |
| 240051007 | X-linked limb girdle muscular dystrophy with normal dystrophin (disorder) | y | direct mapping |
| 240075007 | Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) | y | direct mapping |
| 240078009 | Benign congenital muscular dystrophy with finger flexion contractures (disorder) | y | direct mapping |
| 367621000000103 | Management of multiple sclerosis in stable disability phase (regime/therapy) | y | direct mapping |
| 192928003 | Generalized multiple sclerosis (disorder) | y | direct mapping |
| 193227008 | Pelvic muscular dystrophy (disorder) | y | direct mapping |
| 78468005 | Erb's muscular dystrophy (disorder) | y | direct mapping |
| 278286009 | Right hemiparesis (disorder) | y | direct mapping |
| 275468009 | Congenital quadriplegia (disorder) | y | direct mapping |
| 11538006 | Quadriplegia (disorder) | y | direct mapping |
| 304603007 | Variant Creutzfeldt-Jakob disease (disorder) | y | direct mapping |
| 240070002 | Muscular dystrophy not predominantly limb girdle in distribution (disorder) | y | direct mapping |
| 192819000 | Cerebral degeneration due to progressive multifocal leukoencephalopathy (disorder) | y | direct mapping |
| 230367007 | Neuraxonal leucodystrophy (disorder) | y | direct mapping |
| 442344002 | Dementia due to Huntington chorea (disorder) | y | direct mapping |
| 230255008 | Madras-type motor neurone disease (disorder) | y | direct mapping |
| 844521000000102 | Lindop Parkinson's assessment scale (assessment scale) | y | direct mapping |
| 86044005 | Amyotrophic lateral sclerosis (disorder) | y | direct mapping |
| 313434001 | Residual hemiplegia (disorder) | y | direct mapping |
| 811881000000109 | Multiple sclerosis care plan agreed (finding) | y | direct mapping |
| 924261000000104 | Referral to community Parkinson's disease clinical nurse specialist (procedure) | y | direct mapping |
| 230702001 | Lacunar ataxic hemiparesis (disorder) | y | direct mapping |
| 39058009 | Lumbosacral radiculoplexus neuropathy co-occurrent and due to diabetes mellitus (disorder) | y | direct mapping |
| 240069003 | Late onset proximal muscular dystrophy with dysarthria (disorder) | y | direct mapping |
| 111501005 | Congenital hereditary muscular dystrophy (disorder) | y | direct mapping |
| 230778001 | Monoplegic cerebral palsy affecting lower limb (disorder) | y | direct mapping |
| 367651000000108 | Management of multiple sclerosis in progressive disability phase (regime/therapy) | y | direct mapping |
| 81211007 | Primary lateral sclerosis (disorder) | y | direct mapping |
| 198491000000106 | Multiple sclerosis review (regime/therapy) | y | direct mapping |
| 278287000 | Left hemiparesis (disorder) | y | direct mapping |
| 111508004 | Emery-Dreifuss muscular dystrophy (disorder) | y | direct mapping |
| 278512001 | Ataxic cerebral palsy (disorder) | y | direct mapping |
| 50582007 | Hemiplegia (disorder) | y | direct mapping |
| 166411000000100 | Specialised services for patients with multiple sclerosis - enhanced services administration (procedure) | y | direct mapping |
| 240059009 | Congenital muscular dystrophy (disorder) | y | direct mapping |
| 426373005 | Relapsing remitting multiple sclerosis (disorder) | y | direct mapping |
| 707621005 | Gross motor function classification system for cerebral palsy (assessment scale) | y | direct mapping |
| 230373008 | Chronic progressive multiple sclerosis (disorder) | y | direct mapping |
| 20022000 | Hemiparesis (disorder) | y | direct mapping |
| 240068006 | Autosomal dominant muscular dystrophy with gene located at 5q31 (disorder) | y | direct mapping |
| 240074006 | Scapulohumeral muscular dystrophy (disorder) | y | direct mapping |
| 23732000 | Primary cerebellar degeneration (disorder) | y | direct mapping |
| 230257000 | Paraneoplastic motor neurone disease (disorder) | y | direct mapping |
| 77097004 | Oculopharyngeal muscular dystrophy (disorder) | y | direct mapping |
| 230241000 | Secondary cerebellar degeneration (disorder) | y | direct mapping |
| 240046001 | Muscular dystrophy with predominantly proximal limb girdle distribution (disorder) | y | direct mapping |
| 192929006 | Exacerbation of multiple sclerosis (disorder) | y | direct mapping |
| 240073000 | Autosomal recessive muscular dystrophy not predominantly limb girdle (disorder) | y | direct mapping |
| 230466004 | Alternating hemiplegia of childhood (disorder) | y | direct mapping |
| 49049000 | Parkinson's disease (disorder) | y | direct mapping |
| 713060000 | Sporadic Creutzfeldt-Jakob disease (disorder) | y | direct mapping |
| 240047005 | X-linked muscular dystrophy with limb girdle distribution (disorder) | y | direct mapping |
| 879471000000102 | Referral to community Parkinson's service (procedure) | y | direct mapping |
| 230687001 | Myopathy in myasthenia gravis (disorder) | y | direct mapping |
| 73297009 | Muscular dystrophy (disorder) | y | direct mapping |
| 230238009 | Progressive spinocerebellar ataxia with retained tendon reflexes (disorder) | y | direct mapping |
| 230564004 | Chronic inflammatory demyelinating polyradiculoneuropathy with central nervous system demyelination (disorder) | y | direct mapping |
| 22255007 | Progressive multifocal leukoencephalopathy (disorder) | y | direct mapping |
| 58756001 | Huntington's chorea (disorder) | y | direct mapping |
| 240049008 | Intermediate X-linked muscular dystrophy (disorder) | y | direct mapping |
| 240062007 | Ullrich congenital muscular dystrophy (disorder) | y | direct mapping |
| 79633009 | Spastic hemiplegia (disorder) | y | direct mapping |
| 428700003 | Primary progressive multiple sclerosis (disorder) | y | direct mapping |
| 862081000000106 | Referral to Parkinson's service (procedure) | y | direct mapping |
| 230781006 | Dystonic/rigid cerebral palsy (disorder) | y | direct mapping |
| 240050008 | Manifesting female carrier of X-linked muscular dystrophy (disorder) | y | direct mapping |
| 240071003 | X-linked muscular dystrophy not predominantly limb girdle (disorder) | y | direct mapping |
| 759091000000105 | Multiple sclerosis monitoring second letter (procedure) | y | direct mapping |
| 759131000000108 | Multiple sclerosis monitoring telephone invitation (procedure) | y | direct mapping |
| 759171000000105 | Multiple sclerosis monitoring third letter (procedure) | y | direct mapping |
| 192965001 | Spastic tetraplegia (disorder) | y | direct mapping |
| 444197004 | Multiple system atrophy, Parkinson variant (disorder) | y | direct mapping |
| 307360006 | Leucodystrophy without a known biochemical basis (disorder) | y | direct mapping |
| 67747009 | Ocular muscular dystrophy (disorder) | y | direct mapping |
| 267604001 | Myasthenic syndrome due to diabetic amyotrophy (disorder) | y | direct mapping |
| 230684008 | Ocular myasthenia (disorder) | y | descendant of concept mapped from leaf |
| 292991000119106 | Eaton Lambert syndrome without underlying malignancy (disorder) | y | descendant of concept mapped from leaf |
| 111503008 | Merosin deficient congenital muscular dystrophy (disorder) | y | descendant of concept mapped from leaf |
| 763829004 | Oculopharyngodistal myopathy (disorder) | y | descendant of concept mapped from leaf |
| 441717007 | Hemiplegia of nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 672441000119103 | Hemiplegia of nondominant side due to and following ischemic cerebrovascular accident (disorder) | y | descendant of concept mapped from leaf |
| 720523006 | Autosomal recessive limb girdle muscular dystrophy type 2K (disorder) | y | descendant of concept mapped from leaf |
| 294111000119107 | Hemiplegia of left nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 702317003 | Chorea-athetoid cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 290481000119100 | Spastic hemiplegia of right dominant side (disorder) | y | descendant of concept mapped from leaf |
| 77956009 | Steinert myotonic dystrophy syndrome (disorder) | y | descendant of concept mapped from leaf |
| 442676003 | Hemiplegia of dominant side as late effect of cerebrovascular disease (disorder) | y | descendant of concept mapped from leaf |
| 732930007 | Autosomal recessive limb girdle muscular dystrophy type 2T (disorder) | y | descendant of concept mapped from leaf |
| 716335003 | Congenital suprabulbar paresis (disorder) | y | descendant of concept mapped from leaf |
| 129620000 | Scapuloperoneal muscular dystrophy (disorder) | y | descendant of concept mapped from leaf |
| 305719002 | Neuromyotonia (disorder) | y | descendant of concept mapped from leaf |
| 716107009 | Early onset parkinsonism and intellectual disability syndrome (disorder) | y | descendant of concept mapped from leaf |
| 726616006 | Autosomal recessive limb girdle muscular dystrophy type 2L (disorder) | y | descendant of concept mapped from leaf |
| 763776004 | Kelch like family member 9 related early-onset distal myopathy (disorder) | y | descendant of concept mapped from leaf |
| 77461000119109 | Myasthenia gravis with exacerbation (disorder) | y | descendant of concept mapped from leaf |
| 64383006 | Werdnig-Hoffmann disease (disorder) | y | descendant of concept mapped from leaf |
| 414927004 | Ocular myasthenia with strabismus (disorder) | y | descendant of concept mapped from leaf |
| 698846009 | Tibial muscular dystrophy (disorder) | y | descendant of concept mapped from leaf |
| 713487008 | Progressive multifocal leukoencephalopathy co-occurrent with human immunodeficiency virus infection (disorder) | y | descendant of concept mapped from leaf |
| 723308003 | Epidermolysis bullosa simplex with muscular dystrophy (disorder) | y | descendant of concept mapped from leaf |
| 44395000 | Spastic tetraplegia with rigidity syndrome (disorder) | y | descendant of concept mapped from leaf |
| 702319000 | Bilateral cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 903741000000102 | Uhthoff phenomenon (disorder) | y | descendant of concept mapped from leaf |
| 54280009 | Kugelberg-Welander disease (disorder) | y | descendant of concept mapped from leaf |
| 31839002 | Myasthenia gravis, adult form (disorder) | y | descendant of concept mapped from leaf |
| 716662004 | Autosomal dominant late onset Parkinson disease (disorder) | y | descendant of concept mapped from leaf |
| 718179003 | Autosomal recessive limb girdle muscular dystrophy type 2B (disorder) | y | descendant of concept mapped from leaf |
| 230678005 | Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency (disorder) | y | descendant of concept mapped from leaf |
| 230252006 | Oculopharyngeal spinal muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 690271000119104 | Hemiplegia of nondominant side due to and following embolic cerebrovascular accident (disorder) | y | descendant of concept mapped from leaf |
| 230679002 | Abnormality of synaptic vesicles (disorder) | y | descendant of concept mapped from leaf |
| 726614009 | Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) | y | descendant of concept mapped from leaf |
| 240065009 | Adult onset autosomal recessive muscular dystrophy with normal dystrophin (disorder) | y | descendant of concept mapped from leaf |
| 290491000119102 | Spastic hemiplegia of right nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 95647008 | Upper motor neuron disease (disorder) | y | descendant of concept mapped from leaf |
| 442155009 | Hemiplegia of dominant side (disorder) | y | descendant of concept mapped from leaf |
| 55016009 | Congenital muscular hypertrophy-cerebral syndrome (disorder) | y | descendant of concept mapped from leaf |
| 55637002 | Spinal hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 249892007 | Progressive pseudobulbar palsy (disorder) | y | descendant of concept mapped from leaf |
| 718685006 | Orthostatic hypotension co-occurrent and due to Parkinson's disease (disorder) | y | descendant of concept mapped from leaf |
| 41713005 | Benedikt's syndrome (disorder) | y | descendant of concept mapped from leaf |
| 240056002 | Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder) | y | descendant of concept mapped from leaf |
| 49793008 | Hereditary motor neuron disease (disorder) | y | descendant of concept mapped from leaf |
| 702318008 | Mixed cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 34209003 | Cerebral hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 430959006 | Paralytic syndrome of dominant side as late effect of stroke (disorder) | y | descendant of concept mapped from leaf |
| 111506000 | Distal muscular dystrophy, Miyoshi type (disorder) | y | descendant of concept mapped from leaf |
| 230248006 | Scapuloperoneal spinal muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 294121000119100 | Hemiplegia of right dominant side (disorder) | y | descendant of concept mapped from leaf |
| 723612001 | Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) | y | descendant of concept mapped from leaf |
| 726615005 | Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder) | y | descendant of concept mapped from leaf |
| 719989007 | Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | y | descendant of concept mapped from leaf |
| 43486001 | Hemiplegic cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 702321005 | Pentaplegic cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 240077004 | Severe scapuloperoneal muscular dystrophy with cardiomyopathy (disorder) | y | descendant of concept mapped from leaf |
| 703524005 | Spinal muscular atrophy with progressive myoclonic epilepsy (disorder) | y | descendant of concept mapped from leaf |
| 294041000119107 | Flaccid hemiplegia of left dominant side (disorder) | y | descendant of concept mapped from leaf |
| 733490006 | Distal myopathy with early respiratory muscle involvement (disorder) | y | descendant of concept mapped from leaf |
| 294101000119109 | Hemiplegia of left dominant side (disorder) | y | descendant of concept mapped from leaf |
| 82178003 | Neonatal myasthenia gravis (disorder) | y | descendant of concept mapped from leaf |
| 718180000 | Autosomal recessive limb girdle muscular dystrophy type 2I (disorder) | y | descendant of concept mapped from leaf |
| 22443004 | Vestibulocerebellar ataxia (disorder) | y | descendant of concept mapped from leaf |
| 84590007 | Lower motor neuron disease (disorder) | y | descendant of concept mapped from leaf |
| 732929002 | Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) | y | descendant of concept mapped from leaf |
| 7379000 | Pseudobulbar palsy (disorder) | y | descendant of concept mapped from leaf |
| 715429006 | Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) | y | descendant of concept mapped from leaf |
| 719987009 | Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) | y | descendant of concept mapped from leaf |
| 140281000119108 | Hemipares as late effect of cerebrovascular disease (disorder) | y | descendant of concept mapped from leaf |
| 276221006 | Millard-Gubler syndrome (disorder) | y | descendant of concept mapped from leaf |
| 398432008 | Bulbar weakness (disorder) | y | descendant of concept mapped from leaf |
| 702316007 | Choreic cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 230251004 | Scapulohumeral spinal muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 766764008 | X-linked distal spinal muscular atrophy type 3 (disorder) | y | descendant of concept mapped from leaf |
| 764944006 | Congenital muscular dystrophy type 1B (disorder) | y | descendant of concept mapped from leaf |
| 717964007 | Juvenile primary lateral sclerosis (disorder) | y | descendant of concept mapped from leaf |
| 725042001 | Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) | y | descendant of concept mapped from leaf |
| 77015008 | Crossed hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 442733008 | Hemiplegia as late effect of cerebrovascular accident (disorder) | y | descendant of concept mapped from leaf |
| 420554003 | Progressive multifocal leukoencephalopathy associated with acquired immunodeficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 441722007 | Spastic hemiplegia of nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 764812008 | Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) | y | descendant of concept mapped from leaf |
| 85505000 | Adult spinal muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia (disorder) | y | descendant of concept mapped from leaf |
| 715565004 | Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) | y | descendant of concept mapped from leaf |
| 733489002 | Distal myopathy with posterior leg and anterior hand involvement (disorder) | y | descendant of concept mapped from leaf |
| 702315006 | Dystonic cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 330421000119102 | Lacunar ataxic hemiparesis of right nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 726618007 | Autosomal recessive limb girdle muscular dystrophy type 2M (disorder) | y | descendant of concept mapped from leaf |
| 1670004 | Cerebral hemiparesis (disorder) | y | descendant of concept mapped from leaf |
| 88923002 | Progressive muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 95650006 | Transient hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 77471000119103 | Myasthenia gravis without exacerbation (disorder) | y | descendant of concept mapped from leaf |
| 703537008 | Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (disorder) | y | descendant of concept mapped from leaf |
| 294131000119102 | Hemiplegia of right nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 702314005 | Non-spastic cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 230264003 | Troyer syndrome (disorder) | y | descendant of concept mapped from leaf |
| 430947007 | Paralytic syndrome of nondominant side as late effect of stroke (disorder) | y | descendant of concept mapped from leaf |
| 31097004 | Post poliomyelitis syndrome (disorder) | y | descendant of concept mapped from leaf |
| 230676009 | Putative defect in acetylcholine synthesis or packaging (disorder) | y | descendant of concept mapped from leaf |
| 292851000119109 | Lacunar ataxic hemiparesis of right dominant side (disorder) | y | descendant of concept mapped from leaf |
| 718178006 | Autosomal dominant limb girdle muscular dystrophy type 1B (disorder) | y | descendant of concept mapped from leaf |
| 733193001 | Dementia co-occurrent and due to progressive multifocal leukoencephalopathy (disorder) | y | descendant of concept mapped from leaf |
| 29951000119107 | Ataxic hemiparesis (disorder) | y | descendant of concept mapped from leaf |
| 240061000 | Congenital muscular dystrophy with arthrogryposis multiplex congenita (disorder) | y | descendant of concept mapped from leaf |
| 230674007 | Pseudomyopathic myasthenia (disorder) | y | descendant of concept mapped from leaf |
| 715340002 | Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) | y | descendant of concept mapped from leaf |
| 46251005 | Corticospinal motor disease (disorder) | y | descendant of concept mapped from leaf |
| 726107008 | Distal myopathy Welander type (disorder) | y | descendant of concept mapped from leaf |
| 111504002 | Walker-Warburg congenital muscular dystrophy (disorder) | y | descendant of concept mapped from leaf |
| 230677000 | Congenital end-plate acetylcholinesterase deficiency (disorder) | y | descendant of concept mapped from leaf |
| 725043006 | Autosomal recessive limb girdle muscular dystrophy type 2O (disorder) | y | descendant of concept mapped from leaf |
| 72655000 | Alternating hypoglossal hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 720522001 | Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) | y | descendant of concept mapped from leaf |
| 719985001 | Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | y | descendant of concept mapped from leaf |
| 82361000119107 | Altered behavior in Huntington's dementia (disorder) | y | descendant of concept mapped from leaf |
| 702383005 | Distal myopathy 2 (disorder) | y | descendant of concept mapped from leaf |
| 722987009 | Amyotrophic lateral sclerosis plus syndrome (disorder) | y | descendant of concept mapped from leaf |
| 427027005 | Lumbosacral radiculoplexus neuropathy co-occurrent and due to type 2 diabetes mellitus (disorder) | y | descendant of concept mapped from leaf |
| 702343002 | Early onset myopathy with fatal cardiomyopathy (disorder) | y | descendant of concept mapped from leaf |
| 101421000119107 | Dementia due to Parkinson's disease (disorder) | y | descendant of concept mapped from leaf |
| 5262007 | Spinal muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 763533003 | Distal hereditary motor neuropathy Jerash type (disorder) | y | descendant of concept mapped from leaf |
| 672461000119104 | Hemiplegia of dominant side due to and following ischemic cerebrovascular accident (disorder) | y | descendant of concept mapped from leaf |
| 84160009 | Laryngeal hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 230253001 | Bulbospinal neuronopathy (disorder) | y | descendant of concept mapped from leaf |
| 32162001 | Facial hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 230670003 | Familial infantile myasthenia (disorder) | y | descendant of concept mapped from leaf |
| 725420009 | Congenital muscular dystrophy Paradas type (disorder) | y | descendant of concept mapped from leaf |
| 725146001 | Atypical juvenile parkinsonism (disorder) | y | descendant of concept mapped from leaf |
| 292861000119106 | Lacunar ataxic hemiparesis of left dominant side (disorder) | y | descendant of concept mapped from leaf |
| 765197008 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (disorder) | y | descendant of concept mapped from leaf |
| 294061000119106 | Flaccid hemiplegia of right dominant side (disorder) | y | descendant of concept mapped from leaf |
| 230683002 | Transient neonatal myasthenia (disorder) | y | descendant of concept mapped from leaf |
| 17409003 | Facial hemiparesis (disorder) | y | descendant of concept mapped from leaf |
| 724761004 | Sporadic Parkinson disease (disorder) | y | descendant of concept mapped from leaf |
| 715345007 | Young onset Parkinson disease (disorder) | y | descendant of concept mapped from leaf |
| 718572004 | Bethlem myopathy (disorder) | y | descendant of concept mapped from leaf |
| 723621000 | Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome (disorder) | y | descendant of concept mapped from leaf |
| 290461000119109 | Spastic hemiplegia of left dominant side (disorder) | y | descendant of concept mapped from leaf |
| 441991000 | Hemiparesis as late effect of cerebrovascular accident (disorder) | y | descendant of concept mapped from leaf |
| 240072005 | Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder) | y | descendant of concept mapped from leaf |
| 230249003 | Facioscapulohumeral spinal muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 764859001 | Laing early-onset distal myopathy (disorder) | y | descendant of concept mapped from leaf |
| 719990003 | Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | y | descendant of concept mapped from leaf |
| 699866005 | Progressive bulbar palsy with sensorineural deafness (disorder) | y | descendant of concept mapped from leaf |
| 427571000 | Lumbosacral radiculoplexus neuropathy co-occurrent and due to type 1 diabetes mellitus (disorder) | y | descendant of concept mapped from leaf |
| 718176005 | Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) | y | descendant of concept mapped from leaf |
| 240055003 | Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein (disorder) | y | descendant of concept mapped from leaf |
| 230250003 | Facioscapulohumeral spinal muscular atrophy with sensory loss (disorder) | y | descendant of concept mapped from leaf |
| 608874000 | Eaton Lambert syndrome with underlying malignancy (disorder) | y | descendant of concept mapped from leaf |
| 230246005 | Progressive bulbar palsy of childhood (disorder) | y | descendant of concept mapped from leaf |
| 702320006 | Triplegic cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 711483003 | Spinal muscular atrophy with respiratory distress type 1 (disorder) | y | descendant of concept mapped from leaf |
| 719986000 | Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) | y | descendant of concept mapped from leaf |
| 55051001 | Myasthenia gravis, juvenile form (disorder) | y | descendant of concept mapped from leaf |
| 80976008 | Myasthenic crisis (disorder) | y | descendant of concept mapped from leaf |
| 129596006 | Menopausal muscular dystrophy syndrome (disorder) | y | descendant of concept mapped from leaf |
| 442024001 | Hemiplegia as late effect of cerebrovascular disease (disorder) | y | descendant of concept mapped from leaf |
| 230673001 | Congenital end-plate acetylcholine receptor deficiency (disorder) | y | descendant of concept mapped from leaf |
| 128212001 | Spinal muscular atrophy, type II (disorder) | y | descendant of concept mapped from leaf |
| 719988004 | Autosomal dominant limb girdle muscular dystrophy type 1E (disorder) | y | descendant of concept mapped from leaf |
| 29093005 | Crossed hemiparesis (disorder) | y | descendant of concept mapped from leaf |
| 230671004 | Acetylcholine resynthesis deficiency (disorder) | y | descendant of concept mapped from leaf |
| 294051000119109 | Flaccid hemiplegia of left nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 441892008 | Spastic hemiplegia of dominant side (disorder) | y | descendant of concept mapped from leaf |
| 85672005 | Anterior horn cell disease (disorder) | y | descendant of concept mapped from leaf |
| 733028000 | Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (disorder) | y | descendant of concept mapped from leaf |
| 16171003 | Double athetosis (disorder) | y | descendant of concept mapped from leaf |
| 442077006 | Flaccid hemiplegia of nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 111500006 | Muscular dystrophy-deafmutism syndrome (disorder) | y | descendant of concept mapped from leaf |
| 442020005 | Flaccid hemiplegia of dominant side (disorder) | y | descendant of concept mapped from leaf |
| 715341003 | Autosomal recessive limb girdle muscular dystrophy type 2A (disorder) | y | descendant of concept mapped from leaf |
| 763718009 | Finnish upper limb onset distal myopathy (disorder) | y | descendant of concept mapped from leaf |
| 724778008 | Progressive relapsing multiple sclerosis (disorder) | y | descendant of concept mapped from leaf |
| 404689008 | Alternating hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 763067000 | Autosomal dominant congenital benign spinal muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 230258005 | Amyotrophic lateral sclerosis with dementia (disorder) | y | descendant of concept mapped from leaf |
| 763314009 | Congenital muscular dystrophy with hyperlaxity (disorder) | y | descendant of concept mapped from leaf |
| 864471000000106 | Anterior opercular syndrome (disorder) | y | descendant of concept mapped from leaf |
| 766246000 | Marburg acute multiple sclerosis (disorder) | y | descendant of concept mapped from leaf |
| 718177001 | Autosomal recessive limb girdle muscular dystrophy type 2F (disorder) | y | descendant of concept mapped from leaf |
| 718555006 | Juvenile amyotrophic lateral sclerosis (disorder) | y | descendant of concept mapped from leaf |
| 56409008 | Monoplegic cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 371079004 | Paraplegic cerebral palsy (disorder) | y | descendant of concept mapped from leaf |
| 330411000119109 | Lacunar ataxic hemiparesis of left nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 163601006 | On examination - hemiplegia (disorder) | y | descendant of concept mapped from leaf |
| 290471000119103 | Spastic hemiplegia of left nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 294071000119100 | Flaccid hemiplegia of right nondominant side (disorder) | y | descendant of concept mapped from leaf |
| 724820006 | Functional hemiparesis (disorder) | y | descendant of concept mapped from leaf |
| 719836007 | X-linked distal arthrogryposis multiplex congenita (disorder) | y | descendant of concept mapped from leaf |
| 725907002 | Autosomal recessive limb girdle muscular dystrophy type 2Y (disorder) | y | descendant of concept mapped from leaf |
| 726617002 | Autosomal recessive limb girdle muscular dystrophy type 2N (disorder) | y | descendant of concept mapped from leaf |
| 230247001 | Distal spinal muscular atrophy (disorder) | y | descendant of concept mapped from leaf |
| 732931006 | Autosomal recessive limb girdle muscular dystrophy type 2R (disorder) | y | descendant of concept mapped from leaf |
| 718850008 | Autosomal recessive limb girdle muscular dystrophy type 2E (disorder) | y | descendant of concept mapped from leaf |
| 240053005 | Hereditary myopathy limited to females (disorder) | y | descendant of concept mapped from leaf |
| 442668000 | Hemiplegia of nondominant side as late effect of cerebrovascular disease (disorder) | y | descendant of concept mapped from leaf |
| 230784003 | Congenital pseudobulbar palsy (disorder) | y | descendant of concept mapped from leaf |
| 904541000000109 | Bilateral spastic cerebral palsy | n | via Query Table |
| 198881000000107 | Multiple sclerosis care plan agreed (procedure) | n | via Query Table |
| 367571000000100 | Management of multiple sclerosis in onset phase | n | via Query Table |
| 367601000000107 | Management of multiple sclerosis in early disease phase | n | via Query Table |
| 368791000000106 | Malignant multiple sclerosis | n | via Query Table |
| 230776002 | Cerebral palsy with spastic/ataxic diplegia (disorder) | n | via Query Table |
| 249852005 | Spastic quadriplegia (disorder) | n | via Query Table |
| 922071000000105 | Sporadic Creutzfeldt Jakob disease | n | via Query Table |
| 924271000000106 | Referral to community Parkinson's disease clinical nurse specialist | n | via Query Table |
| 654381000000101 | Congenital hereditary muscular dystrophy NOS (disorder) | n | via Query Table |
| 879481000000100 | Referral to community Parkinson's service | n | via Query Table |
| 778171000000101 | Postpolio syndrome | n | via Query Table |
| 881481000000108 | Gross Motor Function Classification System | n | via Query Table |
| 307781000000109 | Worster - Drought syndrome (disorder) | n | via Query Table |
| 907161000000106 | Seen by Parkinson's service | n | via Query Table |
| 909641000000107 | Dystonic cerebral palsy (disorder) | n | via Query Table |
| 639721000000103 | Myasthenic syndrome due to other malignancy (disorder) | n | via Query Table |
| 207291000000109 | Multiple sclerosis care plan agreed | n | via Query Table |
| 1032661000000100 | Multiple system atrophy, Parkinson variant (disorder) | n | via Query Table |
| 367691000000100 | Management of multiple sclerosis in palliative phase | n | via Query Table |
| 1178005 | Infantile spastic cerebral palsy (disorder) | n | via Query Table |
| 367611000000109 | Management of multiple sclerosis in early disease phase | n | via Query Table |
| 368781000000109 | Benign multiple sclerosis | n | via Query Table |
| 207751000000108 | Hemiparesis | n | via Query Table |
| 477771000000108 | [X]Parkinsonism in diseases classified elsewhere (disorder) | n | via Query Table |
| 343571000000103 | Malignant multiple sclerosis (disorder) | n | via Query Table |
| 368801000000105 | Primary progressive multiple sclerosis | n | via Query Table |
| 68078001 | Mixed congenital myopathy (disorder) | n | via Query Table |
| 275469001 | Congenital diplegia (disorder) | n | via Query Table |
| 724997001 | Lumbosacral plexopathy co-occurrent and due to diabetes mellitus (disorder) | n | via Query Table |
| 213631000000103 | Multiple sclerosis review | n | via Query Table |
| 207281000000107 | Multiple sclerosis care plan agreed | n | via Query Table |
| 23488005 | AIDS with progressive multifocal leukoencephalopathy (disorder) | n | via Query Table |
| 757061000000109 | Neuromyotonia | n | via Query Table |
| 213641000000107 | Multiple sclerosis multidisciplinary review | n | via Query Table |
| 759141000000104 | Multiple sclerosis monitoring telephone invitation | n | via Query Table |
| 91213008 | Neonatal myasthenia (disorder) | n | via Query Table |
| 468231000000107 | [X]Other myasthenic syndromes in neoplastic disease classified elsewhere (disorder) | n | via Query Table |
| 367671000000104 | Management of multiple sclerosis in progressive disability phase | n | via Query Table |
| 16092000 | Cord multiple sclerosis (disorder) | n | via Query Table |
| 1032651000000103 | Multiple system atrophy, cerebellar variant | n | via Query Table |
| 343601000000105 | Secondary progressive multiple sclerosis (disorder) | n | via Query Table |
| 171451000000101 | Specialised services for patients with multiple sclerosis - enhanced services administration | n | via Query Table |
| 343591000000104 | Relapsing and remitting multiple sclerosis (disorder) | n | via Query Table |
| 759101000000102 | Multiple sclerosis monitoring second letter | n | via Query Table |
| 230774004 | Cerebral palsy with spastic tetraparesis (disorder) | n | via Query Table |
| 449831000000105 | [X]Other infantile cerebral palsy (disorder) | n | via Query Table |
| 583151000000109 | Other anterior horn cell disease (disorder) | n | via Query Table |
| 479161000000109 | [X]Dementia in Parkinson's disease (disorder) | n | via Query Table |
| 230374002 | Remittent-progressive multiple sclerosis (disorder) | n | via Query Table |
| 759181000000107 | Multiple sclerosis monitoring third letter | n | via Query Table |
| 432561000000107 | [X]Myasthenic syndromes in endocrine diseases classified elsewhere (disorder) | n | via Query Table |
| 630711000000100 | Myasthenic syndrome due to disease NOS (disorder) | n | via Query Table |
| 213651000000105 | Multiple sclerosis multidisciplinary review | n | via Query Table |
| 463581000000100 | [X]Myasthenic syndromes in other diseases classified elsewhere (disorder) | n | via Query Table |
| 785861000000101 | Referral to community multiple sclerosis team | n | via Query Table |
| 368811000000107 | Relapsing and remitting multiple sclerosis | n | via Query Table |
| 213621000000100 | Multiple sclerosis review | n | via Query Table |
| 587911000000102 | Hereditary progressive muscular dystrophy NOS (disorder) | n | via Query Table |
| 343541000000109 | Benign multiple sclerosis (disorder) | n | via Query Table |
| 833421000000101 | Spastic hemiplegic cerebral palsy | n | via Query Table |
| 832861000000102 | Spastic quadriplegic cerebral palsy | n | via Query Table |
| 862091000000108 | Referral to Parkinson's service | n | via Query Table |
| 412291000000109 | [X]Other spinal muscular atrophies and related syndromes (disorder) | n | via Query Table |
| 1032671000000107 | Multiple system atrophy, Parkinson variant | n | via Query Table |
| 832711000000109 | Cerebral palsy | n | via Query Table |
| 1032641000000101 | Multiple system atrophy, cerebellar variant (disorder) | n | via Query Table |
| 368821000000101 | Secondary progressive multiple sclerosis | n | via Query Table |
| 199721000000105 | Hemiparesis NOS (disorder) | n | via Query Table |
| 864481000000108 | Anterior opercular syndrome | n | via Query Table |
| 814231000000109 | Spastic quadriplegic cerebral palsy (disorder) | n | via Query Table |
| 371119007 | Quadriplegic spastic cerebral palsy (disorder) | n | via Query Table |
| 275467004 | Congenital spastic cerebral palsy (disorder) | n | via Query Table |
| 275466008 | Congenital cerebral palsy (disorder) | n | via Query Table |
| 586591000000100 | Multiple sclerosis NOS (disorder) | n | via Query Table |
| 832701000000107 | Cerebral palsy | n | via Query Table |
| 192177005 | [X]Dementia in Parkinson's disease (disorder) | n | via Query Table |
| 367641000000105 | Management of multiple sclerosis in stable disability phase | n | via Query Table |
| 759061000000104 | Multiple sclerosis monitoring first letter | n | via Query Table |
| 192957004 | Ataxic infantile cerebral palsy (disorder) | n | via Query Table |
| 756881000000108 | History of Parkinson's disease | n | via Query Table |
| 309461000000102 | Worster-Drought syndrome | n | via Query Table |
| 832721000000103 | Cerebral palsy | n | via Query Table |
| 368771000000107 | Cerebral degeneration in Parkinson's disease | n | via Query Table |
| 430031000000107 | [X]Other inherited spinal muscular atrophy (disorder) | n | via Query Table |
| 240079001 | Distal muscular dystrophy with adult onset (disorder) | n | via Query Table |
| 176111000000101 | Specialised services for patients with multiple sclerosis - enhanced services administration | n | via Query Table |
| 408371000000100 | [X]Cerebral palsy and other paralytic syndromes (disorder) | n | via Query Table |
| 367631000000101 | Management of multiple sclerosis in stable disability phase | n | via Query Table |
| 376191000000104 | Diabetic amyotrophy (disorder) | n | via Query Table |
| 758991000000103 | Multiple sclerosis monitoring administration | n | via Query Table |
| 584961000000107 | Congenital diplegia NOS (disorder) | n | via Query Table |
| 639671000000108 | Other limb girdle muscular dystrophy (disorder) | n | via Query Table |
| 844531000000100 | Lindop Parkinson's assessment scale | n | via Query Table |
| 18353007 | Brain stem multiple sclerosis (disorder) | n | via Query Table |
| 367661000000106 | Management of multiple sclerosis in progressive disability phase | n | via Query Table |
| 630471000000103 | Anterior horn cell disease NOS (disorder) | n | via Query Table |
| 584951000000109 | Hemiplegia NOS (disorder) | n | via Query Table |
| 881471000000106 | Gross Motor Function Classification System for Cerebral Palsy (assessment scale) | n | via Query Table |
| 343581000000101 | Primary progressive multiple sclerosis (disorder) | n | via Query Table |
| 922061000000103 | Sporadic Creutzfeldt-Jakob disease (disorder) | n | via Query Table |
| 646201000000105 | Motor neurone disease NOS (disorder) | n | via Query Table |
| 762641000000106 | Adult-onset autosomal dominant leucodystrophy (disorder) | n | via Query Table |
| 692711000000106 | Infantile hemiplegia NOS (disorder) | n | via Query Table |
| 192835007 | Parkinsonism with orthostatic hypotension (disorder) | n | via Query Table |
| 367701000000100 | Management of multiple sclerosis in palliative phase | n | via Query Table |
| 230772000 | Infantile cerebral palsy (disorder) | n | via Query Table |
| 367581000000103 | Management of multiple sclerosis in onset phase | n | via Query Table |
| 891211000000104 | Choreoathetoid cerebral palsy | n | via Query Table |
Codes not in the full codelist are in faint grey.