Schizophrenia - CISMeF

Preferred Label : Schizophrenia;

NCIt related terms : Schizophrenia, unspecified;

NCIt definition : A major psychotic disorder characterized by abnormalities in the perception or expression of reality. It affects the cognitive and psychomotor functions. Common clinical signs and symptoms include delusions, hallucinations, disorganized thinking, and retreat from reality.;

Alternative definition : NCI-GLOSS: A group of severe mental disorders in which a person has trouble telling the difference between real and unreal experiences, thinking logically, having normal emotional responses to others, and behaving normally in social situations. Symptoms include seeing, hearing, feeling things that are not there, having false ideas about what is taking place or who one is, nonsense speech, unusual behavior, lack of emotion, and social withdrawal.;

Codes from synonyms : CDR0000450117; F20.9;

Details

Origin ID

C3362;

UMLS CUI

C0036341;

Currated CISMeF NLP mapping
- Schizophrenia [PASCAL descriptor]
- Schizophrenia [ICD-10 category]
- Schizophrenia [LOINC component]
- Schizophrenia [DSM-IV term]
- Schizophrenia [ICD-11 Category]
- Schizophrenia [PASCAL theme]
- Schizophrenia [FRANCIS theme]
- Schizophrenia [ICD-10 category (who)]
- Schizophrenia [HPO term]
- Schizophrenia [MedDRA Preferred Term]
- Schizophrenia [OMIM Phenotype]
- Schizophrenia [ORDO Disease]
- Schizophrenia (disorder) [SNOMED CT concept]
- Schizophrenia NOS [MedDRA LLT]
- Schizophrenia, unspecified [ICD-10 Sub-category (who)]
- Schizophrenia, unspecified [ICD-10 Sub-category]
- schizophrenia [DO Concept]
- schizophrenia [Disease (Nov.)]
- schizophrenia [ICPC-2 Rubric]
- schizophrenia [MedlinePlus Topic]
- schizophrenia [MeSH Descriptor]
- schizophrenia [MeSH concept]
- schizophrenia, nos [SNOMED Notion]
DO Cross reference
- schizophrenia [DO Concept]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Dementia praecox [MedDRA LLT]
- Other transitory neonatal endocrine disorders [ICD-10 category (who)]
- Schizophrenia [ORDO Disease]
- Schizophrenia [LOINC component]
- Schizophrenia [OMIM Phenotype]
- Schizophrenia [ICD-10 category]
- Schizophrenia [HPO term]
- Schizophrenia [PASCAL descriptor]
- Schizophrenia [DSM-IV term]
- Schizophrenia [ICD-11 Category]
- Schizophrenia [ICD-10 category (who)]
- Schizophrenia [MedDRA Preferred Term]
- Schizophrenia (disorder) [SNOMED CT concept]
- Schizophrenia NOS [MedDRA LLT]
- Schizophrenia, unspecified [ICD-10 Sub-category]
- Schizophrenia, unspecified [ICD-10 Sub-category (who)]
- Schizophrenia, unspecified | Other [ICD-10 Subdivision (who)]
- Schizophrenic disorders [ICD-9 code]
- Schizophrenic disorders (disorder) [SNOMED CT concept]
- Unspecified schizophrenia [MedDRA LLT]
- Unspecified schizophrenia [ICD-9 code]
- Unspecified schizophrenia, unspecified [ICD-9 code]
- Unspecified schizophrenia, unspecified state [MedDRA LLT]
- schizophrenia [DO Concept]
- schizophrenia [Disease (Nov.)]
- schizophrenia [ICPC-2 Rubric]
- schizophrenia [MedlinePlus Topic]
- schizophrenia [MeSH Descriptor]
- schizophrenia [MeSH concept]
- schizophrenia, nos [SNOMED Notion]
associated_with_malfunction_of_gene_product
- Astrotactin-2 [NCIt concept]
- D(2) Dopamine Receptor [NCIt concept]
- Myelin Transcription Factor 1-Like Protein [NCIt concept]
concept_is_in_subset
- CPTAC Codelists Terminology [NCIt concept]
- CPTAC Medical Conditions Codelist [NCIt concept]
- CPTAC Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- mCode Elixhauser Psychosis Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_associated_gene
- ASTN2 Gene [NCIt concept]
- ASTN2 wt Allele [NCIt concept]
- DRD2 1 Allele [NCIt concept]
- DRD2 2 Allele [NCIt concept]
- DRD2 Gene [NCIt concept]
- DRD2 wt Allele [NCIt concept]
- HTR2A 1 Allele [NCIt concept]
- HTR2A 2 Allele [NCIt concept]
- HTR2A Gene [NCIt concept]
- HTR2A wt Allele [NCIt concept]
- MIR198 Gene [NCIt concept]
- MIR198 wt Allele [NCIt concept]
- MIR206 Gene [NCIt concept]
- MIR206 wt Allele [NCIt concept]
- MYT1L Gene [NCIt concept]
- MYT1L wt Allele [NCIt concept]
- NRXN1 Gene [NCIt concept]
- NRXN1 wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

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