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Schizophrenia 8(SCZD8)

MedGen UID:: 400456
•Concept ID:: C1864124
•: Mental or Behavioral Dysfunction

Synonyms:	SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 18-RELATED; SCZD8

Monarch Initiative:	MONDO:0011298
OMIM®:	603206

Definition

A schizophrenia that has material basis in an autosomal dominant mutation of SCZD8 on chromosome 18p. [from MONDO]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVSchizophrenia
- CROGVChromosome 2p16.3 deletion syndrome
- CROGVSchizophrenia 1
- CROGVSchizophrenia 2
- CROGVSchizophrenia 3
- CROGVSchizophrenia 4
- CROGVSchizophrenia 5
- CROGVSchizophrenia 6
- CROGVSchizophrenia 7
- CROGVSchizophrenia 8
- CROGVSchizophrenia 9
- CROGVSchizophrenia 10
- CROGVSchizophrenia 11
- CROGVSchizophrenia 12
- CROGVSchizophrenia 13
- CROGVSchizophrenia 14
- CROGVSchizophrenia 15
- CROGVSchizophrenia 16
- CROGVSchizophrenia 18
- CROGVSchizophrenia 19

Abnormality of the nervous system
- Abnormal nervous system physiology
  - Abnormality of mental function
    - Abnormal experience of reality
      - Abnormal psychotic pattern
        Schizophrenia
        Schizophrenia 8

Supplemental Content

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Clinical resources

Molecular resources

Coriell Institute for Medical Research

Consumer resources

Reviews

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