Other Neurological Conditions
Codelist metadata
-
Coding system
- CTV3 (Read V3)
-
Coding system release
- unknown
-
Organisation
- OpenSAFELY
-
Codelist ID
- opensafely/other-neurological-conditions
-
Version Tag
- 2020-06-02
-
Version ID
- 71bb8ca2
Versions
About
Description
Codes indicating other neurological conditions not including stroke or dementia
Methodology
TODO
References
- Discussion on GitHub issue
- Thomas, S (2020). COVID-19 risk group - Neurological disease codelist. [Data Collection]. https://doi.org/10.17037/DATA.00001704
Signed off by
- Laurie Tomlinson, (April 21, 2020)
- Helen McDonald, (April 22, 2020)
- Henry Drysdale, (June 2, 2020)
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.
| 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.