SCZD2
MCID: SCH085
MIFTS: 33
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Schizophrenia 2 (SCZD2)
Categories:
Genetic diseases, Mental diseases, Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Schizophrenia 2:
Classifications:
MalaCards categories:
Global: Genetic diseases Rare diseases Anatomical: Mental diseases Neuronal diseases |
UniProtKB/Swiss-Prot
:
75
Schizophrenia 2: A complex, multifactorial psychotic disorder or group of disorders characterized by disturbances in the form and content of thought (e.g. delusions, hallucinations), in mood (e.g. inappropriate affect), in sense of self and relationship to the external world (e.g. loss of ego boundaries, withdrawal), and in behavior (e.g bizarre or apparently purposeless behavior). 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. Some patients manifest schizophrenic as well as bipolar disorder symptoms and are often given the diagnosis of schizoaffective disorder.
MalaCards based summary : Schizophrenia 2, also known as sczd2, is related to perrault syndrome 1 and schizophrenia. An important gene associated with Schizophrenia 2 is SCZD2 (Schizophrenia Disorder 2). Affiliated tissues include brain and cerebellum. Disease Ontology : 12 A schizophrenia that has material basis in an autosomal dominant mutation of SCZD2 on chromosome 11q14-q21.
Description from OMIM:
603342
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MalaCards organs/tissues related to Schizophrenia 2:41
Brain,
Cerebellum
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Articles related to Schizophrenia 2:(show all 13)
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Search
GEO
for disease gene expression data for Schizophrenia 2.
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Cellular components related to Schizophrenia 2 according to GeneCards Suite gene sharing:
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