Schizophrenia 9

Preferred Label : Schizophrenia 9;

Symbol : SCZD9;

CISMeF acronym : SCZD9;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Schizophrenia 9 with or without an affective disorder; Schizophrenia susceptibility locus, chromosome 1q42-related;

Prefixed ID : #604906;

Details

Origin ID

604906;

UMLS CUI

C1858050;

Automatic exact mappings (from CISMeF team)
- RGS4 wt Allele [NCIt concept]
- symbol withdrawn SCZD9 [HGNC gene]
Broader ORDO disease(s)
- Schizophrenia [ORDO Disease]
Currated CISMeF NLP mapping
- schizophrenia 9 [DO Concept]
DO Cross reference
- schizophrenia 9 [DO Concept]
Genes related to phenotype
- Disrupted in schizophrenia 1 [OMIM gene]
ORDO concept(s)
- Schizophrenia [ORDO Disease]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- schizophrenia 9 [DO Concept]

Keyword's position in hierarchy(ies) :

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