Neurological disorders (not including epilepsy)
- Coding system
- CTV3 (Read V3)
- Coding system release
- unknown
- Organisation
- Office for National Statistics
- Codelist ID
- ons/neurological-disorders-not-including-epilepsy
- Version ID
- 22dbd4f7
Versions
- 22dbd4f7
No metadata has been provided for this codelist.
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| A411. | Creutzfeldt-Jakob disease |
| A413. | Progressive multifocal leucoencephalopathy |
| Eu022 | [X]Dementia in Huntington's disease |
| Eu023 | [X]Dementia in Parkinson's disease |
| F0301 | Subacute sclerosing panencephalitis |
| F11x7 | Cerebral degeneration due to Creutzfeldt-Jakob disease |
| F11x8 | Cerebral degeneration due to multifocal leucoencephalopathy |
| F12.. | Parkinson's disease |
| F12z. | Parkinson's disease NOS |
| F1304 | Progressive supranuclear palsy |
| F134. | Huntington's disease |
| F140. | Friedreich ataxia |
| F142. | Primary cerebellar degeneration |
| F142z | Primary cerebellar degeneration NOS |
| F1440 | Alcoholic cerebellar degeneration |
| F152. | Motor neurone disease |
| F1522 | Progressive bulbar palsy |
| F1524 | Primary lateral sclerosis |
| F152z | Motor neurone disease NOS |
| F20.. | Multiple sclerosis |
| F200. | Multiple sclerosis of the brainstem |
| F201. | Multiple sclerosis of the spinal cord |
| F202. | Generalised multiple sclerosis |
| F203. | Exacerbation of multiple sclerosis |
| F20z. | Multiple sclerosis NOS |
| F210. | Optic neuromyelitis |
| F211. | (Schilder's disease) or (Balo's concentric sclerosis) |
| F22.. | (Hemiplegia) or (hemiparesis) |
| F220. | Flaccid hemiplegia |
| F221. | (Spastic hemiplegia) or (spastic foot) |
| F222. | Left: [hemiplegia] or [sided weakness] |
| F223. | Right: [hemiplegia] or [sided weakness] |
| F22z. | Hemiplegia NOS |
| F23.. | Congenital cerebral palsy (& spastic) |
| F231. | Infantile hemiplegia |
| F234. | Infantile hemiplegia NOS |
| F23y. | Other congenital cerebral palsy |
| F23y0 | Ataxic infantile cerebral palsy |
| F23y1 | Hypotonic cerebral palsy |
| F23yz | Other infantile cerebral palsy NOS |
| F23z. | Congenital cerebral palsy NOS |
| F240. | Quadriplegia |
| F380. | Myasthenia gravis |
| F3800 | Persistent neonatal myasthenia gravis |
| F3801 | Juvenile or adult myasthenia gravis |
| F380z | Myasthenia gravis NOS |
| F381. | Myasthenic syndrome due to disease EC |
| F3810 | Eaton Lambert myasthenic syndrome |
| F3813 | (Myasth syndr due to diab amyotroph) or (diab amyotroph) |
| F383. | Congenital and developmental myasthenia |
| F390. | Congenital hereditary muscular dystrophy |
| F390z | Congenital hereditary muscular dystrophy NOS |
| F391. | Hereditary progressive muscular dystrophy |
| F3910 | Duchenne muscular dystrophy |
| F3911 | Erb's muscular dystrophy |
| F3912 | Pelvic muscular dystrophy |
| F3913 | Other limb girdle muscular dystrophy |
| F3914 | Facioscapulohumeral muscular dystrophy |
| F3915 | Distal muscular dystrophy with juvenile onset |
| F3916 | Ocular muscular dystrophy |
| F3917 | Oculopharyngeal muscular dystrophy |
| F3918 | Becker muscular dystrophy |
| F391y | (Oth specif hered progress musc dystrophy) or (distal dystr) |
| F391z | Hereditary progressive muscular dystrophy NOS |
| F39B. | Muscular dystrophy |
| Fyu84 | [X]Other myasthenic syndromes in neoplastic disease CE |
| Fyu85 | [X]Myasthenic syndromes/other diseases classified elsewhere |
| Fyu90 | [X]Other infantile cerebral palsy |
| G669. | Cerebral palsy, not congenital or infantile, acute |
| X002R | Prog spinocerebellar ataxia with retained tendon reflexes |
| X002U | Secondary cerebellar degeneration |
| X002i | Western Pacific motor neurone disease |
| X002j | Madras-type motor neurone disease |
| X002l | Paraneoplastic motor neurone disease |
| X003a | Juvenile Parkinson's disease |
| X003p | Juvenile onset Huntington's disease |
| X003q | Late onset Huntington's disease |
| X003r | Akinetic-rigid form of Huntington's disease |
| X005Q | Neuraxonal leucodystrophy |
| X005c | Acute relapsing multiple sclerosis |
| X005d | Chronic progressive multiple sclerosis |
| X005e | Remittent-progressive multiple sclerosis |
| X005l | Balo concentric sclerosis |
| X007Q | Alternating hemiplegia of childhood |
| X00AX | Chr inflamm demyelinat polyradiculoneuropathy with cns demye |
| X00Cb | Genetically determined myasthenia |
| X00Ce | Congenital myasthenia |
| X00Cu | Myasthenia gravis associated with thymoma |
| X00Cv | Generalised myasthenia |
| X00Cw | Myopathy in myasthenia gravis |
| X00DE | Lacunar ataxic hemiparesis |
| X00Em | Infantile cerebral palsy |
| X00En | Spastic cerebral palsy |
| X00Eo | Cerebral palsy with spastic tetraparesis |
| X00Eq | Cerebral palsy with spastic/ataxic diplegia |
| X00Er | Monoplegic cerebral palsy affecting upper limb |
| X00Es | Monoplegic cerebral palsy affecting lower limb |
| X00Eu | Dyskinetic cerebral palsy |
| X00Ew | Dystonic/rigid cerebral palsy |
| X40VL | Late infantile metachromatic leucodystrophy |
| X40VM | Juvenile metachromatic leucodystrophy |
| X40VN | Adult metachromatic leucodystrophy |
| X708H | Muscular dystrophy with predom proximl limb girdle distribut |
| X708I | X-linked muscular dystrophy with limb girdle distribution |
| X708J | X-linked muscular dystrophy with abnormal dystrophin |
| X708K | Intermediate X-linked muscular dystrophy |
| X708L | Manifesting female carrier of X-linked muscular dystrophy |
| X708M | X-linked limb girdle muscul dystrophy with normal dystrophin |
| X708N | Ji muscular dystrophy |
| X708P | Autosomal recess muscular dystrophy with limb girdle distrib |
| X708S | Fukuyama muscular dystrophy |
| X708T | Autosomal recess muscular dystrophy with gene located at 15q |
| X708U | Reunion-Indiana Amish type muscular dystrophy |
| X708V | Congenital muscular dystrophy |
| X708W | Western type of congenital muscular dystrophy |
| X708Y | Ullrich congenital muscular dystrophy |
| X708Z | Eichsfeld type congenital muscular dystrophy |
| X708b | Hutterite type of muscular dystrophy |
| X708d | Autosomal domin muscular dystrophy with limb girdle distrib |
| X708e | Autosomal domin muscular dystrophy with gene located at 5q31 |
| X708f | Late onset proximal muscular dystrophy with dysarthria |
| X708g | Muscular dystrophy not predom limb girdle in distribution |
| X708h | X-linked muscular dystrophy not predominantly limb girdle |
| X708i | Emery-Dreifuss muscular dystrophy |
| X708k | Autosom recessive muscular dystrophy not predom limb girdle |
| X708l | Scapulohumeral muscular dystrophy |
| X708m | Distal muscular dystrophy |
| X708n | Autosomal dominant muscular dystrophy not predom limb girdle |
| X708o | Benign scapuloperoneal muscular dystrophy |
| X708q | Benign congen muscular dystrophy wth finger flex contracture |
| X708r | Distal muscular dystrophy with adult onset |
| X76je | Spastic quadriplegia |
| X76n9 | Hemiparesis |
| XE15T | Hemiplegia |
| XE15U | Spastic hemiplegia |
| XE15n | Myasthenic syndrome due to diabetic amyotrophy |
| XE15p | Other specified hereditary progressive muscular dystrophy |
| XE181 | Cerebral palsy (&/or infantile) &/or infantile hemiplegia |
| XE18Z | Muscular dystrophy (& [Duchenne muscular dystrophy]) |
| XE2Q7 | Athetoid cerebral palsy |
| XE2Q8 | Cerebral palsy |
| XE2Q9 | Cerebral palsy with spastic diplegia |
| XE2se | Cerebral palsy with spastic tetraplegia |
| XM1Pu | Congenital cerebral palsy |
| XM1Pv | Congenital spastic cerebral palsy |
| XM1Pw | Congenital quadriplegia |
| Xa0ON | Severe childhood autosomal recessive muscular dystrophy |
| Xa0ZY | Cerebro-oculo-dysgenesis-muscular dystrophy syndrome |
| Xa0fr | Right hemiplegia |
| Xa0fs | Left hemiplegia |
| Xa0ft | Right hemiparesis |
| Xa0fu | Left hemiparesis |
| Xa0lL | Muscular dystrophy |
| Xa0lM | Ataxic cerebral palsy |
| XaA1S | New variant of Creutzfeldt-Jakob disease |
| XaB4V | Leucodystrophy without a known biochemical basis |
| XaBE2 | Cerebral palsy, not congenital or infantile, acute |
| XaELO | Residual hemiplegia |
| XaKA8 | Specialised services for pts with multiple sclerosis ESA |
| XaKvm | Multiple sclerosis review |
| XaKvn | Multiple sclerosis multidisciplinary review |
| XaKzg | Multiple sclerosis care plan agreed |
| XaL3N | Hemiparesis NOS |
| XaOfZ | Cerebral degeneration in Parkinson's disease |
| XaOzZ | Benign multiple sclerosis |
| XaP0X | Malignant multiple sclerosis |
| XaP0r | Primary progressive multiple sclerosis |
| XaP1B | Relapsing and remitting multiple sclerosis |
| XaP1V | Secondary progressive multiple sclerosis |
| XaPSY | Management of multiple sclerosis in onset phase |
| XaPSZ | Management of multiple sclerosis in early disease phase |
| XaPSa | Management of multiple sclerosis in stable disability phase |
| XaPSb | Management of MS in progressive disability phase |
| XaPSc | Management of multiple sclerosis in palliative phase |
| XaQwf | History of Parkinson's disease |
| XaX9A | Multiple sclerosis monitoring administration |
| XaX9F | Multiple sclerosis monitoring first letter |
| XaX9H | Multiple sclerosis monitoring second letter |
| XaX9J | Multiple sclerosis monitoring telephone invitation |
| XaX9L | Multiple sclerosis monitoring third letter |
| XaXGu | Adult autosomal dominant leucodystrophy |
| XaXsg | Referral to community multiple sclerosis team |
| XaYP3 | Clinically isolated syndrome |
| XaYfK | Spastic hemiplegic cerebral palsy |
| XaYgp | Spastic quadriplegic cerebral palsy |
| XaZYZ | Lindop Parkinson's assessment scale |
| XaZxQ | Referral to Parkinson's service |
| XaaRV | Referral to community Parkinson's service |
| XaaVG | Gross Motor Function Classification System Cerebral Palsy |
| XaadE | Choreoathetoid cerebral palsy |
| Xab3R | Bilateral spastic cerebral palsy |
| Xab7w | Seen by Parkinson's disease service |
| XabVp | Sporadic Creutzfeldt-Jakob disease |
| XabbC | Referral to community Parkinson disease clin nurse spcialist |
| XaeUM | Multiple system atrophy, cerebellar variant |
| XaeUN | Multiple system atrophy, Parkinson variant |
| Y1015 | Multiple Sclerosis |
| Y10b7 | Multiple Sclerosis |
| Y1f23 | Multiple sclerosis monitoring invitation |
| Y3466 | Hemiplegic |
Codes not in the full codelist are in faint grey.