Schizophrenia - CISMeF

Preferred Label : Schizophrenia;

Symbol : SCZD;

CISMeF acronym : SCZD;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Schizophrenia with or without an affective disorder;

Description : Schizophrenia is a psychosis, a disorder of thought and sense of self. Although it affects emotions, it is distinguished from mood disorders in which such disturbances are primary. Similarly, there may be mild impairment of cognitive function, and it is distinguished from the dementias in which disturbed cognitive function is considered primary. There is no characteristic pathology, such as neurofibrillary tangles in Alzheimer disease (104300). Schizophrenia is a common disorder with a lifetime prevalence of approximately 1%. It is highly heritable but the genetics are complex. This may not be a single entity. - Reviews In a review of schizophrenia, van Os and Kapur (2009) noted that in Japan the term schizophrenia was abandoned and the illness is now called integration-dysregulation syndrome.;

Inheritance : Autosomal dominant;

Laboratory abnormalities : Abnormal EEG in 25% hospitalized patients;

Prefixed ID : #181500;

Détails

Origin ID

181500;

UMLS CUI

C0036341;

Currated CISMeF NLP mapping
- Schizophrenia [PASCAL descriptor]
- Schizophrenia [ICD-10 category]
- 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 [NCIt concept]
- Schizophrenia [ORDO Disease]
- Schizophrenia [LOINC component]
- Schizophrenia (disorder) [SNOMED CT concept]
- Schizophrenia NOS [MedDRA LLT]
- Schizophrenia, unspecified [ICD-10 Sub-category]
- schizophrenia [Disease (Nov.)]
- schizophrenia [DO Concept]
- schizophrenia [ICPC-2 Rubric]
- schizophrenia [MedlinePlus Topic]
- schizophrenia [MeSH Descriptor]
- schizophrenia [MeSH concept]
- schizophrenia, nos [SNOMED Notion]
DO Cross reference
- schizophrenia [DO Concept]
Genes related to phenotype
- 5,10-methylenetetrahydrofolate reductase [OMIM gene]
- 5-hydroxytryptamine receptor 2a [OMIM gene]
- Chitinase 3-like 1 [OMIM gene]
- Dopamine receptor d3 [OMIM gene]
- Reticulon 4 receptor [OMIM gene]
- Synapsin II [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Delusions [HPO term]
- EEG abnormality [HPO term]
- Hallucinations [HPO term]
- Heterogeneous [HPO term]
- Negativism [HPO term]
- Schizophrenia [HPO term]
- Social and occupational deterioration [HPO term]
ORDO concept(s)
- Schizophrenia [ORDO Disease]
See also inter- (CISMeF)
- schizoaffective disorder [Disease (Nov.)]
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 [ICD-10 category (who)]
- Schizophrenia [LOINC component]
- Schizophrenia [MedDRA Preferred Term]
- Schizophrenia [ORDO Disease]
- Schizophrenia [NCIt concept]
- Schizophrenia [ICD-10 category]
- Schizophrenia [HPO term]
- Schizophrenia [DSM-IV term]
- Schizophrenia [PASCAL descriptor]
- Schizophrenia [ICD-11 Category]
- Schizophrenia (disorder) [SNOMED CT concept]
- Schizophrenia NOS [MedDRA LLT]
- Schizophrenia, unspecified [ICD-10 Sub-category (who)]
- Schizophrenia, unspecified [ICD-10 Sub-category]
- 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 [ICPC-2 Rubric]
- schizophrenia [MedlinePlus Topic]
- schizophrenia [MeSH Descriptor]
- schizophrenia [MeSH concept]
- schizophrenia [DO Concept]
- schizophrenia [Disease (Nov.)]
- schizophrenia, nos [SNOMED Notion]

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