Log In|Sign Up
ENChromosome 2p16.3 Deletion Syndrome (SCZD17)
Alias:
Schizophrenia 17
Schizophrenia Susceptibility Locus Chromosome 2p16-Related
Schizophrenia, Susceptibility to, 17
Schizophrenia, Type 17
Sczd17
Favorite
Chromosome 2p16.3 Deletion Syndrome, is also known as schizophrenia 17. An important gene associated with Chromosome 2p16.3 Deletion Syndrome is NRXN1 (Neurexin 1). Affiliated tissues include cingulate cortex and brain.
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
