Other Neurological Conditions



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
  • 2020-06-02

Description

Codes indicating other neurological conditions not including stroke or dementia

Methodology

TODO

References

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.