chromosome 2p16.3 deletion syndrome
Go to external page https://bio.scai.fraunhofer.de/ontology/schizophrenia#chromosome_2p16.3_deletion_syndrome
This is just here as a test because I lose it
Term information
oboInOwl:hasDefinition
Deletions at 2p16.3 involving exons of NRXN1 are associated with susceptibility to autism, schizophrenia (SCZD17), developmental delay, intellectual disability, and dysmorphic features.
seeAlso
https://pdfs.semanticscholar.org/8d8f/c922f1673763fa25244fcc7e68160403d019.pdf?_ga=2.131809551.1247871322.1566453399-2137029120.1566453399