Other Neurological Conditions (SNOMED) Draft



Coding system
SNOMED CT
Project
OpenSAFELY
Codelist ID
opensafely/other-neurological-conditions-snomed
Version
2020-06-02-draft

Description

Automatically-generated equivalent of Other Neurological Conditions

Methodology

See code on GitHub

References

  • ...

Signed off by

  • ...

This definition has been computed by taking the manually created full codelist and converting it to a list of rules that define the codelist.

Active Concepts
Inactive Concepts
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 in the definition are underlined. Codes in the full codelist are in blue. Related codes not in the codelist are in black.