Automatically-generated equivalent of Other Neurological Conditions
See code on GitHub
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 Concepts448054001)
361273006)
361272001)
192818008)
192819000)
and all descendants
341551000000108)
128188000)
and all descendants except:
783005002)
230564004)
425390006)
and all descendants
442344002)
and all descendants
56989000)
and all descendants
10394003)
707621005)
20022000)
and all descendants
50582007)
and all descendants except:
771304005)
515841000000104)
58756001)
and all descendants
792004)
230702001)
and all descendants
844521000000102)
39058009)
and all descendants
367591000000101)
367561000000107)
367681000000102)
367651000000108)
367621000000103)
24326000)
44359008)
47683004)
37340000)
and all descendants except:
784341001)
838276009)
784391002)
772129007)
770430000)
771302009)
770630005)
771081007)
230274000)
783618006)
785809005)
866051002)
771238004)
770727008)
771475006)
24700007)
and all descendants except:
816984002)
811881000000109)
758981000000100)
759051000000102)
759091000000105)
759131000000108)
759171000000105)
198491000000106)
and all descendants
444197004)
444024002)
73297009)
and all descendants except:
770792007)
771334000)
783554002)
771272007)
787037000)
783176002)
771267003)
783174004)
782772000)
783175003)
783166000)
782675008)
783148005)
785298001)
784352007)
91637004)
and all descendants except:
770596007)
193209005)
267604001)
230687001)
230367007)
49049000)
and all descendants
23732000)
and all descendants
22255007)
and all descendants
230238009)
28978003)
11538006)
862081000000106)
and all descendants
924261000000104)
785851000000104)
230241000)
907151000000108)
307324001)
192965001)
723621000)
166411000000100)
713060000)
192685000)
304603007)
23488005)
762641000000106)
630471000000103)
864481000000108)
192957004)
240057006)
368781000000109)
343541000000109)
904541000000109)
18353007)
368771000000107)
832721000000103)
832711000000109)
832701000000107)
230774004)
230776002)
891211000000104)
230373008)
193216006)
275466008)
275469001)
584961000000107)
654381000000101)
240059009)
275467004)
16092000)
376191000000104)
240079001)
733490006)
909641000000107)
192928003)
881481000000108)
881471000000106)
207751000000108)
199721000000105)
584951000000109)
587911000000102)
756881000000108)
230772000)
692711000000106)
1178005)
307360006)
93153005)
844531000000100)
724997001)
368791000000106)
343571000000103)
367601000000107)
367611000000109)
367581000000103)
367571000000100)
367701000000100)
367691000000100)
367671000000104)
367661000000106)
367641000000105)
367631000000101)
68078001)
646201000000105)
586591000000100)
207281000000107)
207291000000109)
198881000000107)
758991000000103)
759061000000104)
759101000000102)
759141000000104)
759181000000107)
213641000000107)
213651000000105)
213621000000100)
213631000000103)
1032671000000107)
1032661000000100)
1032651000000103)
1032641000000101)
630711000000100)
639721000000103)
91213008)
757061000000109)
583151000000109)
639671000000108)
192835007)
778171000000101)
368801000000105)
343581000000101)
371119007)
862091000000108)
924271000000106)
879481000000100)
785861000000101)
368811000000107)
343591000000104)
230374002)
368821000000101)
343601000000105)
907161000000106)
240056002)
833421000000101)
249852005)
832861000000102)
814231000000109)
176111000000101)
171451000000101)
922071000000105)
922061000000103)
307781000000109)
309461000000102)
408371000000100)
192177005)
479161000000109)
432561000000107)
463581000000100)
449831000000105)
430031000000107)
468231000000107)
412291000000109)
477771000000108)
| 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.