Codes indicating other neurological conditions not including stroke or dementia
TODO
This definition has been computed by taking the manually created full codelist and converting it to a list of rules that define the codelist.
F22..)
F3813)
F221.)
XaXGu)
X40VN)
F1440)
X007Q)
Xa0lM)
and all descendants
Xab3R)
F11x7)
F11x8)
XaOfZ)
XE2Q8)
XE181)
XE2Q9)
X00Eo)
XE2se)
and all descendants
X00Eq)
G669.)
XaBE2)
Xa0ZY)
X00AX)
F383.)
XM1Pu)
F23..)
F23z.)
X00Ce)
XM1Pv)
A411.)
and all descendants
X00Eu)
and all descendants
F3810)
F140.)
X00Cv)
and all descendants
X00Cb)
XaaVG)
X76n9)
and all descendants
XE15T)
and all descendants
XaQwf)
F134.)
and all descendants
F23y1)
X00Em)
and all descendants
F231.)
and all descendants
X003a)
X40VM)
F3801)
X00DE)
X40VL)
XaB4V)
XaZYZ)
X002j)
XaPSb)
XaPSZ)
XaPSY)
XaPSc)
XaPSa)
X00Es)
X00Er)
F152.)
F152z)
F20..)
and all descendants
XaKzg)
XaX9A)
and all descendants
XaKvm)
and all descendants
XaeUN)
XaeUM)
F39B.)
Xa0lL)
and all descendants except:
X708c)
X708Q)
F3900)
X708j)
X708X)
X708O)
X708a)
X708R)
X708p)
F380.)
F380z)
XE15n)
F381.)
X00Cw)
X005Q)
F23y.)
F23yz)
X002l)
F12..)
F12z.)
F3800)
F142.)
F142z)
F1524)
X002R)
F1522)
A413.)
F1304)
F240.)
XaZxQ)
and all descendants
XabbC)
XaXsg)
X002U)
Xab7w)
X00En)
XaYfK)
X76je)
XaYgp)
XaKA8)
F0301)
X002i)
Eu022)
Eu023)
Fyu85)
Fyu84)
| CTV3ID | CTV3PreferredTermDesc | CTV3Source |
|---|---|---|
| F390. | Congenital hereditary muscular dystrophy | CTV3Map_Code_And_Term |
| F390z | Congenital hereditary muscular dystrophy NOS | CTV3Map_Code_And_Term |
| F391. | Hereditary progressive muscular dystrophy | CTV3Map_Code_And_Term |
| F3910 | Duchenne muscular dystrophy | CTV3Map_Code_And_Term |
| F3910 | Duchenne muscular dystrophy | CTV3Map_Code_Only |
| F3911 | Erb's muscular dystrophy | CTV3Map_Code_And_Term |
| F3912 | Pelvic muscular dystrophy | CTV3Map_Code_And_Term |
| F3913 | Other limb girdle muscular dystrophy | CTV3Map_Code_And_Term |
| F3914 | Facioscapulohumeral muscular dystrophy | CTV3Map_Code_And_Term |
| F3914 | Facioscapulohumeral muscular dystrophy | CTV3Map_Code_Only |
| F3915 | Distal muscular dystrophy with juvenile onset | CTV3Map_Code_And_Term |
| F3916 | Ocular muscular dystrophy | CTV3Map_Code_And_Term |
| F3917 | Oculopharyngeal muscular dystrophy | CTV3Map_Code_And_Term |
| F3918 | Becker muscular dystrophy | CTV3Map_Code_And_Term |
| F391y | (Oth specif hered progress musc dystrophy) or (distal dystr) | CTV3_Children |
| F391z | Hereditary progressive muscular dystrophy NOS | CTV3Map_Code_And_Term |
| F39B. | Muscular dystrophy | High_Level_SNOMED |
| X005Q | Neuraxonal leucodystrophy | High_Level_SNOMED |
| X40VL | Late infantile metachromatic leucodystrophy | CTV3_Children |
| X40VM | Juvenile metachromatic leucodystrophy | CTV3_Children |
| X40VN | Adult metachromatic leucodystrophy | CTV3_Children |
| X708H | Muscular dystrophy with predom proximl limb girdle distribut | CTV3_Children |
| X708I | X-linked muscular dystrophy with limb girdle distribution | CTV3_Children |
| X708J | X-linked muscular dystrophy with abnormal dystrophin | CTV3_Children |
| X708K | Intermediate X-linked muscular dystrophy | CTV3_Children |
| X708L | Manifesting female carrier of X-linked muscular dystrophy | CTV3_Children |
| X708M | X-linked limb girdle muscul dystrophy with normal dystrophin | CTV3_Children |
| X708N | Ji muscular dystrophy | CTV3_Children |
| X708P | Autosomal recess muscular dystrophy with limb girdle distrib | CTV3_Children |
| X708S | Fukuyama muscular dystrophy | CTV3_Children |
| X708T | Autosomal recess muscular dystrophy with gene located at 15q | CTV3_Children |
| X708U | Reunion-Indiana Amish type muscular dystrophy | CTV3_Children |
| X708V | Congenital muscular dystrophy | CTV3_Children |
| X708W | Western type of congenital muscular dystrophy | CTV3_Children |
| X708Y | Ullrich congenital muscular dystrophy | CTV3_Children |
| X708Z | Eichsfeld type congenital muscular dystrophy | CTV3_Children |
| X708b | Hutterite type of muscular dystrophy | CTV3_Children |
| X708d | Autosomal domin muscular dystrophy with limb girdle distrib | CTV3_Children |
| X708e | Autosomal domin muscular dystrophy with gene located at 5q31 | CTV3_Children |
| X708f | Late onset proximal muscular dystrophy with dysarthria | CTV3_Children |
| X708g | Muscular dystrophy not predom limb girdle in distribution | CTV3_Children |
| X708h | X-linked muscular dystrophy not predominantly limb girdle | CTV3_Children |
| X708i | Emery-Dreifuss muscular dystrophy | CTV3Map_Code_And_Term |
| X708k | Autosom recessive muscular dystrophy not predom limb girdle | CTV3_Children |
| X708l | Scapulohumeral muscular dystrophy | CTV3_Children |
| X708m | Distal muscular dystrophy | CTV3Map_Code_And_Term |
| X708m | Distal muscular dystrophy | CTV3Map_Code_Only |
| X708n | Autosomal dominant muscular dystrophy not predom limb girdle | CTV3_Children |
| X708o | Benign scapuloperoneal muscular dystrophy | CTV3_Children |
| X708q | Benign congen muscular dystrophy wth finger flex contracture | CTV3_Children |
| X708r | Distal muscular dystrophy with adult onset | CTV3_Children |
| XE15p | Other specified hereditary progressive muscular dystrophy | CTV3Map_Code_And_Term |
| XE15p | Other specified hereditary progressive muscular dystrophy | CTV3Map_Code_Only |
| XE18Z | Muscular dystrophy (& [Duchenne muscular dystrophy]) | CTV3_Children |
| Xa0ON | Severe childhood autosomal recessive muscular dystrophy | CTV3_Children |
| Xa0ZY | Cerebro-oculo-dysgenesis-muscular dystrophy syndrome | High_Level_SNOMED |
| Xa0lL | Muscular dystrophy | CTV3Map_Code_And_Term |
| XaB4V | Leucodystrophy without a known biochemical basis | High_Level_SNOMED |
| XaXGu | Adult autosomal dominant leucodystrophy | CTV3_Children |
| F23.. | Congenital cerebral palsy (& spastic) | CTV3_Children |
| F23y. | Other congenital cerebral palsy | CTV3_Children |
| F23y0 | Ataxic infantile cerebral palsy | CTV3Map_Code_And_Term |
| F23y1 | Hypotonic cerebral palsy | CTV3Map_Code_And_Term |
| F23yz | Other infantile cerebral palsy NOS | CTV3_Children |
| F23z. | Congenital cerebral palsy NOS | CTV3_Children |
| Fyu90 | [X]Other infantile cerebral palsy | CTV3_Children |
| G669. | Cerebral palsy, not congenital or infantile, acute | CTV3_Children |
| X00Em | Infantile cerebral palsy | CTV3_Children |
| X00En | Spastic cerebral palsy | CTV3_Children |
| X00Eo | Cerebral palsy with spastic tetraparesis | CTV3_Children |
| X00Eq | Cerebral palsy with spastic/ataxic diplegia | CTV3Map_Code_And_Term |
| X00Er | Monoplegic cerebral palsy affecting upper limb | CTV3_Children |
| X00Es | Monoplegic cerebral palsy affecting lower limb | CTV3_Children |
| X00Eu | Dyskinetic cerebral palsy | CTV3_Children |
| X00Ew | Dystonic/rigid cerebral palsy | CTV3_Children |
| XE181 | Cerebral palsy (&/or infantile) &/or infantile hemiplegia | CTV3_Children |
| XE2Q7 | Athetoid cerebral palsy | CTV3_Children |
| XE2Q8 | Cerebral palsy | CTV3Map_Code_And_Term |
| XE2Q9 | Cerebral palsy with spastic diplegia | CTV3Map_Code_And_Term |
| XE2Q9 | Cerebral palsy with spastic diplegia | CTV3Map_Code_Only |
| XE2se | Cerebral palsy with spastic tetraplegia | CTV3_Children |
| XM1Pu | Congenital cerebral palsy | CTV3_Children |
| XM1Pv | Congenital spastic cerebral palsy | CTV3_Children |
| Xa0lM | Ataxic cerebral palsy | CTV3_Children |
| XaBE2 | Cerebral palsy, not congenital or infantile, acute | CTV3Map_Code_And_Term |
| XaYfK | Spastic hemiplegic cerebral palsy | CTV3Map_Code_And_Term |
| XaYgp | Spastic quadriplegic cerebral palsy | CTV3Map_Code_And_Term |
| XaaVG | Gross Motor Function Classification System Cerebral Palsy | CTV3Map_Code_And_Term |
| XaadE | Choreoathetoid cerebral palsy | CTV3Map_Code_And_Term |
| XaadE | Choreoathetoid cerebral palsy | CTV3Map_Code_Only |
| Xab3R | Bilateral spastic cerebral palsy | CTV3_Children |
| A411. | Creutzfeldt-Jakob disease | CTV3Map_Code_And_Term |
| F11x7 | Cerebral degeneration due to Creutzfeldt-Jakob disease | CTV3Map_Code_And_Term |
| XaA1S | New variant of Creutzfeldt-Jakob disease | CTV3_Children |
| XabVp | Sporadic Creutzfeldt-Jakob disease | CTV3_Children |
| F22.. | (Hemiplegia) or (hemiparesis) | High_Level_SNOMED |
| F220. | Flaccid hemiplegia | CTV3Map_Code_And_Term |
| F221. | (Spastic hemiplegia) or (spastic foot) | High_Level_SNOMED |
| F222. | Left: [hemiplegia] or [sided weakness] | CTV3_Children |
| F223. | Right: [hemiplegia] or [sided weakness] | CTV3_Children |
| F22z. | Hemiplegia NOS | CTV3Map_Code_And_Term |
| F231. | Infantile hemiplegia | CTV3Map_Code_And_Term |
| F234. | Infantile hemiplegia NOS | CTV3Map_Code_And_Term |
| X007Q | Alternating hemiplegia of childhood | High_Level_SNOMED |
| X00DE | Lacunar ataxic hemiparesis | CTV3_Children |
| X76n9 | Hemiparesis | CTV3Map_Code_Only |
| XE15T | Hemiplegia | CTV3Map_Code_And_Term |
| XE15U | Spastic hemiplegia | CTV3Map_Code_And_Term |
| Xa0fr | Right hemiplegia | CTV3Map_Code_And_Term |
| Xa0fs | Left hemiplegia | CTV3Map_Code_And_Term |
| Xa0ft | Right hemiparesis | CTV3Map_Code_Only |
| Xa0fu | Left hemiparesis | CTV3Map_Code_Only |
| XaELO | Residual hemiplegia | CTV3_Children |
| XaL3N | Hemiparesis NOS | CTV3_Children |
| Y3466 | Hemiplegic | CTV3_Children |
| Eu022 | [X]Dementia in Huntington's disease | CTV3Map_Code_And_Term |
| F134. | Huntington's disease | CTV3Map_Code_And_Term |
| X003p | Juvenile onset Huntington's disease | CTV3_Children |
| X003q | Late onset Huntington's disease | CTV3_Children |
| X003r | Akinetic-rigid form of Huntington's disease | CTV3_Children |
| F1304 | Progressive supranuclear palsy | CTV3Map_Code_And_Term |
| F1304 | Progressive supranuclear palsy | CTV3Map_Code_Only |
| F152. | Motor neurone disease | CTV3Map_Code_And_Term |
| F1522 | Progressive bulbar palsy | CTV3Map_Code_And_Term |
| F1524 | Primary lateral sclerosis | CTV3Map_Code_And_Term |
| F152z | Motor neurone disease NOS | CTV3Map_Code_And_Term |
| X002i | Western Pacific motor neurone disease | CTV3_Children |
| X002j | Madras-type motor neurone disease | CTV3_Children |
| X002l | Paraneoplastic motor neurone disease | CTV3_Children |
| F20.. | Multiple sclerosis | CTV3Map_Code_And_Term |
| F20.. | Multiple sclerosis | CTV3Map_Code_Only |
| F200. | Multiple sclerosis of the brainstem | CTV3Map_Code_And_Term |
| F201. | Multiple sclerosis of the spinal cord | CTV3Map_Code_And_Term |
| F202. | Generalised multiple sclerosis | CTV3Map_Code_And_Term |
| F203. | Exacerbation of multiple sclerosis | CTV3Map_Code_And_Term |
| F20z. | Multiple sclerosis NOS | CTV3Map_Code_And_Term |
| X005c | Acute relapsing multiple sclerosis | CTV3_Children |
| X005d | Chronic progressive multiple sclerosis | CTV3_Children |
| X005e | Remittent-progressive multiple sclerosis | CTV3_Children |
| X00AX | Chr inflamm demyelinat polyradiculoneuropathy with cns demye | High_Level_SNOMED |
| XaKA8 | Specialised services for pts with multiple sclerosis ESA | CTV3Map_Code_And_Term |
| XaKvm | Multiple sclerosis review | CTV3Map_Code_And_Term |
| XaKvn | Multiple sclerosis multidisciplinary review | CTV3Map_Code_And_Term |
| XaKzg | Multiple sclerosis care plan agreed | CTV3Map_Code_And_Term |
| XaOzZ | Benign multiple sclerosis | CTV3Map_Code_And_Term |
| XaP0X | Malignant multiple sclerosis | CTV3_Children |
| XaP0r | Primary progressive multiple sclerosis | CTV3Map_Code_And_Term |
| XaP1B | Relapsing and remitting multiple sclerosis | CTV3Map_Code_And_Term |
| XaP1V | Secondary progressive multiple sclerosis | CTV3Map_Code_And_Term |
| XaPSY | Management of multiple sclerosis in onset phase | CTV3Map_Code_And_Term |
| XaPSZ | Management of multiple sclerosis in early disease phase | CTV3Map_Code_And_Term |
| XaPSa | Management of multiple sclerosis in stable disability phase | CTV3Map_Code_And_Term |
| XaPSb | Management of MS in progressive disability phase | CTV3Map_Code_And_Term |
| XaPSc | Management of multiple sclerosis in palliative phase | CTV3Map_Code_And_Term |
| XaX9A | Multiple sclerosis monitoring administration | CTV3Map_Code_And_Term |
| XaX9F | Multiple sclerosis monitoring first letter | CTV3Map_Code_And_Term |
| XaX9H | Multiple sclerosis monitoring second letter | CTV3Map_Code_And_Term |
| XaX9J | Multiple sclerosis monitoring telephone invitation | CTV3Map_Code_And_Term |
| XaX9L | Multiple sclerosis monitoring third letter | CTV3_Children |
| XaXsg | Referral to community multiple sclerosis team | CTV3Map_Code_And_Term |
| F380. | Myasthenia gravis | CTV3Map_Code_And_Term |
| F3800 | Persistent neonatal myasthenia gravis | CTV3_Children |
| F3801 | Juvenile or adult myasthenia gravis | CTV3Map_Code_And_Term |
| F380z | Myasthenia gravis NOS | CTV3Map_Code_And_Term |
| F381. | Myasthenic syndrome due to disease EC | CTV3Map_Code_And_Term |
| F3810 | Eaton Lambert myasthenic syndrome | CTV3Map_Code_And_Term |
| F3810 | Eaton Lambert myasthenic syndrome | CTV3Map_Code_Only |
| F3813 | (Myasth syndr due to diab amyotroph) or (diab amyotroph) | High_Level_SNOMED |
| F383. | Congenital and developmental myasthenia | CTV3Map_Code_And_Term |
| Fyu84 | [X]Other myasthenic syndromes in neoplastic disease CE | CTV3_Children |
| Fyu85 | [X]Myasthenic syndromes/other diseases classified elsewhere | CTV3_Children |
| X00Cb | Genetically determined myasthenia | CTV3_Children |
| X00Ce | Congenital myasthenia | CTV3_Children |
| X00Cu | Myasthenia gravis associated with thymoma | CTV3_Children |
| X00Cv | Generalised myasthenia | CTV3_Children |
| X00Cw | Myopathy in myasthenia gravis | CTV3_Children |
| XE15n | Myasthenic syndrome due to diabetic amyotrophy | CTV3Map_Code_And_Term |
| XE15n | Myasthenic syndrome due to diabetic amyotrophy | CTV3Map_Code_Only |
| Eu023 | [X]Dementia in Parkinson's disease | CTV3Map_Code_And_Term |
| F12.. | Parkinson's disease | CTV3Map_Code_And_Term |
| F12z. | Parkinson's disease NOS | CTV3Map_Code_And_Term |
| X003a | Juvenile Parkinson's disease | CTV3_Children |
| XaOfZ | Cerebral degeneration in Parkinson's disease | CTV3Map_Code_And_Term |
| XaQwf | History of Parkinson's disease | CTV3Map_Code_And_Term |
| XaZYZ | Lindop Parkinson's assessment scale | CTV3Map_Code_And_Term |
| XaZxQ | Referral to Parkinson's service | CTV3Map_Code_And_Term |
| XaaRV | Referral to community Parkinson's service | CTV3Map_Code_And_Term |
| Xab7w | Seen by Parkinson's disease service | CTV3Map_Code_And_Term |
| XabbC | Referral to community Parkinson disease clin nurse spcialist | CTV3Map_Code_And_Term |
| XaeUN | Multiple system atrophy, Parkinson variant | CTV3_Children |
| F140. | Friedreich ataxia | CTV3Map_Code_And_Term |
| F142. | Primary cerebellar degeneration | CTV3Map_Code_And_Term |
| F142z | Primary cerebellar degeneration NOS | CTV3Map_Code_And_Term |
| F1440 | Alcoholic cerebellar degeneration | CTV3Map_Code_And_Term |
| X002R | Prog spinocerebellar ataxia with retained tendon reflexes | High_Level_SNOMED |
| X002U | Secondary cerebellar degeneration | High_Level_SNOMED |
| XaeUM | Multiple system atrophy, cerebellar variant | CTV3_Children |
| F240. | Quadriplegia | CTV3Map_Code_And_Term |
| F240. | Quadriplegia | CTV3Map_Code_Only |
| X76je | Spastic quadriplegia | CTV3_Children |
| XM1Pw | Congenital quadriplegia | CTV3Map_Code_And_Term |
| XM1Pw | Congenital quadriplegia | CTV3Map_Code_Only |
| A413. | Progressive multifocal leucoencephalopathy | CTV3Map_Code_And_Term |
| A413. | Progressive multifocal leucoencephalopathy | CTV3Map_Code_Only |
| F0301 | Subacute sclerosing panencephalitis | CTV3Map_Code_And_Term |
| F0301 | Subacute sclerosing panencephalitis | CTV3Map_Code_Only |
| F11x8 | Cerebral degeneration due to multifocal leucoencephalopathy | CTV3Map_Code_And_Term |
Codes not in the full codelist are in faint grey.