second generation antipsychotic
CHEBI:CHEBI_65191
Definition
Antipsychotic drugs which can have different modes of action but which tend to be less likely than first generation antipsychotics to cause extrapyramidal motor control disabilities such as body rigidity or Parkinson's disease-type movements.
Alternative Names
- atypical antipsychotic
- atypical antipsychotic agent
- atypical antipsychotic agents
- atypical antipsychotic drug
- atypical antipsychotic drugs
- atypical antipsychotics
- second generation antipsychotic agent
- second generation antipsychotic agents
- second generation antipsychotic drug
- second generation antipsychotic drugs
- second generation antipsychotics
Treatment Applications
-
hereditary spastic paraplegia 77View Disease →
DOID:0110822
-
hereditary spastic paraplegia 9BView Disease →
DOID:0110825
-
nemaline myopathy 6View Disease →
DOID:0110935
-
myopathy with extrapyramidal signsView Disease →
DOID:0111335
-
progressive myoclonus epilepsy 10View Disease →
DOID:0111445
-
progressive myoclonus epilepsy 9View Disease →
DOID:0111450
-
progressive myoclonus epilepsy 8View Disease →
DOID:0111451
-
familial adult myoclonic epilepsy 1View Disease →
DOID:0111690
-
familial adult myoclonic epilepsy 5View Disease →
DOID:0111691
-
familial adult myoclonic epilepsy 4View Disease →
DOID:0111693
-
familial adult myoclonic epilepsy 7View Disease →
DOID:0111694
-
familial adult myoclonic epilepsy 3View Disease →
DOID:0111695
-
familial adult myoclonic epilepsy 6View Disease →
DOID:0111696
-
Waisman syndromeView Disease →
DOID:0111781
-
X-linked parkinsonism-spasticity syndromeView Disease →
DOID:0112105
-
hereditary spastic paraplegia 82View Disease →
DOID:0112343
-
hereditary spastic paraplegia 79BView Disease →
DOID:0112344
-
hereditary spastic paraplegia 83View Disease →
DOID:0112346
-
hereditary spastic paraplegia 84View Disease →
DOID:0112347
-
hereditary spastic paraplegia 78View Disease →
DOID:0112348
-
progressive bulbar palsyView Disease →
DOID:681
-
spastic monoplegiaView Disease →
DOID:10968
-
Huntington's diseaseView Disease →
DOID:12858
-
hypokalemic periodic paralysisView Disease →
DOID:14452
-
gait apraxiaView Disease →
DOID:4260
-
asymmetric motor neuropathyView Disease →
DOID:7559
-
spastic ataxia 1View Disease →
DOID:0050772
-
spinocerebellar ataxia type 5View Disease →
DOID:0050882
-
Troyer syndromeView Disease →
DOID:0050886
-
spastic ataxia 2View Disease →
DOID:0050941
-
spastic ataxia 3View Disease →
DOID:0050942
-
spastic ataxia 4View Disease →
DOID:0050943
-
spastic ataxia 5View Disease →
DOID:0050944
-
spastic ataxia 7View Disease →
DOID:0050945
-
Charlevoix-Saguenay spastic ataxiaView Disease →
DOID:0050946
-
spastic ataxiaView Disease →
DOID:0050952
-
spinocerebellar ataxia type 8View Disease →
DOID:0050959
-
spinocerebellar ataxia type 12View Disease →
DOID:0050962
-
spinocerebellar ataxia type 13View Disease →
DOID:0050963
-
obsolete spinocerebellar ataxia type 16View Disease →
DOID:0050966
-
spinocerebellar ataxia type 17View Disease →
DOID:0050967
-
spinocerebellar ataxia type 19/22View Disease →
DOID:0050970
-
spinocerebellar ataxia type 21View Disease →
DOID:0050972
-
spinocerebellar ataxia type 23View Disease →
DOID:0050973
-
spinocerebellar ataxia type 31View Disease →
DOID:0050980
-
spinocerebellar ataxia type 35View Disease →
DOID:0050982
-
spinocerebellar ataxia type 40View Disease →
DOID:0050986
-
hypomyelinating leukoencephalopathyView Disease →
DOID:0050987
-
episodic ataxia type 7View Disease →
DOID:0050995
-
episodic ataxia type 8View Disease →
DOID:0050996
-
Renpenning syndromeView Disease →
DOID:0060179
-
pontocerebellar hypoplasia type 1AView Disease →
DOID:0060265
-
pontocerebellar hypoplasia type 2EView Disease →
DOID:0060271
-
Cayman type cerebellar ataxiaView Disease →
DOID:0060694
-
hypomyelinating leukodystrophy 6View Disease →
DOID:0060798
-
late onset Parkinson's diseaseView Disease →
DOID:0060892
-
juvenile-onset Parkinson's diseaseView Disease →
DOID:0060893
-
early-onset Parkinson's diseaseView Disease →
DOID:0060894
-
NESCAV syndromeView Disease →
DOID:0070039
-
paroxysmal nonkinesigenic dyskinesia 3View Disease →
DOID:0070442
-
hereditary spastic paraplegia 87View Disease →
DOID:0070456
-
hereditary spastic paraplegia 88View Disease →
DOID:0070457
-
hereditary spastic paraplegia 89View Disease →
DOID:0070458
-
dopamine transporter deficiency syndromeView Disease →
DOID:0070487
-
obsolete olivopontocerebellar atrophy VView Disease →
DOID:0080017
-
Charcot-Marie-Tooth disease type 5View Disease →
DOID:0080067
-
spastic ataxia 8View Disease →
DOID:0080252
-
myofibrillar myopathy 8View Disease →
DOID:0080308
-
hyperekplexia 4View Disease →
DOID:0080581
-
Fazio-Londe diseaseView Disease →
DOID:0080632
-
arthrogryposis multiplex congenita-3View Disease →
DOID:0080979
-
oculopharyngodistal myopathy 1View Disease →
DOID:0081297
-
oculopharyngodistal myopathy 3View Disease →
DOID:0081299
-
congenital myopathy 9BView Disease →
DOID:0081344
-
congenital myopathy 16View Disease →
DOID:0081348
-
congenital myopathy 19View Disease →
DOID:0081351
-
congenital myopathy 21View Disease →
DOID:0081353
-
congenital myopathy 22BView Disease →
DOID:0081355
-
spastic quadriplegic cerebral palsy 2View Disease →
DOID:0081360
-
spastic quadriplegic cerebral palsy 3View Disease →
DOID:0081361
-
amyotrophic lateral sclerosis type 26View Disease →
DOID:0081380
-
amyotrophic lateral sclerosis type 28View Disease →
DOID:0081382
-
paroxysmal nonkinesigenic dyskinesia 1View Disease →
DOID:0090049
-
dystonia 12View Disease →
DOID:0090056
-
X-linked dystonia-parkinsonismView Disease →
DOID:0090057
-
giant axonal neuropathy 1View Disease →
DOID:0090068
-
giant axonal neuropathy 2View Disease →
DOID:0090069
-
spinal muscular atrophyView Disease →
DOID:12377
-
obsolete hereditary spastic paraplegia 1View Disease →
DOID:0110762
-
hereditary spastic paraplegia 15View Disease →
DOID:0110768
-
hereditary spastic paraplegia 30View Disease →
DOID:0110781
-
hereditary spastic paraplegia 31View Disease →
DOID:0110782
-
hereditary spastic paraplegia 49View Disease →
DOID:0110801
-
hereditary spastic paraplegia 51View Disease →
DOID:0110803
-
hereditary spastic paraplegia 52View Disease →
DOID:0110804
-
hereditary spastic paraplegia 57View Disease →
DOID:0110809
-
hereditary spastic paraplegia 63View Disease →
DOID:0110814
-
hereditary spastic paraplegia 72AView Disease →
DOID:0110817
-
hereditary spastic paraplegia 73View Disease →
DOID:0110818
-
hereditary spastic paraplegia 76View Disease →
DOID:0110821
Drug Classification
-
antipsychotic agentView Class →
CHEBI:35476
Important Medical Information
⚕️ This information is sourced from ChEBI (Chemical Entities of Biological Interest) database and is intended for educational purposes only.
- Always consult with a healthcare professional before starting, stopping, or modifying any medication.
- Side effects may vary and this list may not be comprehensive.
- Drug interactions may occur with other medications.
Additional Identifiers
- core#notation
- CHEBI:65191
🔍 Click on any linked disease name to learn more about the conditions this medication is used to treat, or explore related drug classifications for more information about similar medications.
Additional Attributes
- oboInOwl#hasOBONamespace
- chebi_ontology
- oboInOwl#id
- CHEBI:65191
- core#notation
- CHEBI:65191
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/chebi#3_STAR
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- rdf-schema#range
- https://w3id.org/def/predibionto#has_drug_112766
- RO_0000087
- http://purl.obolibrary.org/obo/CHEBI_71253
- owl#someValuesFrom
- t321154
- owl#annotatedSource
- t269878