Schizophrenia; Sczd
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 (OMIM ). 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.Schizophrenia and bipolar disorder (see {125480}) are generally considered to be separate entities, but patients who exhibit multiple symptoms of both disorders are often given the hybrid diagnosis schizoaffective disorder (Blacker and Tsuang, 1992).
Genes related to Schizophrenia; Sczd
- HTR2A
- CHI3L1
- AKT1
- MTHFR
- APOL2
- APOL4
- DAOA
- SYN2
- DRD3
- DISC2
- RTN4R
Clinical Features
Top most frequent phenotypes and symptoms related to Schizophrenia; Sczd
- Intellectual disability
- Microcephaly
- Behavioral abnormality
- Depressivity
- Dementia
- Autism
- EEG abnormality
- Rigidity
- Anxiety
- Small for gestational age
And another 20 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Schizophrenia; Sczd Is also known as schizophrenia with or without an affective disorder.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Schizophrenia; Sczd Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Serotonin Metabolism Deficiency NGS Panel.
By Fulgent Genetics Fulgent Genetics (United States).
SLC6A4, TPH1, AANAT, TPH2, HTR3C, HTR3E, DDC, HTR1A, HTR1B, HTR2A, HTR2B, HTR2C, HTR3A, HTR3B, HTR5A, HTR6, HTR7
Specificity
6 %
Genes
10 % |
HTR2A.
By Fulgent Genetics Fulgent Genetics (United States).
HTR2A
Specificity
100 %
Genes
10 % |
HTR2A.
By Genelex (United States).
HTR2A
Specificity
100 %
Genes
10 % |
YouScript Psychotropic.
By Genelex (United States).
SLC6A4, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, HTR2A
Specificity
15 %
Genes
10 % |
GeneSight Psychotropic.
By Assurex Health, Inc. (United States).
SLC6A4, UGT1A4, UGT2B15, CYP2B6, CYP2C19, CYP2C9, CYP2D6, CYP3A4, HLA-A, HTR2A
Specificity
10 %
Genes
10 % |
Comprehensive Pharmacogenomics (PGX) Panel.
By ApolloGen, Inc. (United States).
SLCO1B1, VKORC1, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, F5, HTR2A, MTHFR, OPRM1
Specificity
19 %
Genes
19 % |
OneOme RightMed comprehensive test.
By OneOme (United States).
SLCO1B1, SLC6A4, TPMT, UGT1A1, IFNL3, NUDT15, VKORC1, CYP2B6, CYP2C18, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, CYP4F2, DPYD, DRD2, F2, F5, GRIK4 , (...)
View the complete list with 4 more genes
Specificity
5 %
Genes
10 % |
Citalopram response.
By Xcode Life Xcode Life (India).
SLC6A4, CYP2C19, HTR2A
Specificity
34 %
Genes
10 % |
You can get up to 207 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT