Automatically-generated equivalent of Other Neurological Conditions
See code on GitHub
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.