Schizophrenia 13
diseaseOn this page
Also known as schizophrenia susceptibility locus, chromosome 15Q13-q14-relatedschizophrenia, susceptibility to, 13SCZD13
Summary
Schizophrenia 13 (MONDO:0013089) is a disease. A subtype of schizophrenia, susceptibility to — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | schizophrenia 13 |
| Mondo ID | MONDO:0013089 |
| OMIM | 613025 |
| DOID | DOID:0070089 |
| UMLS | C2751663 |
| MedGen | 416605 |
| Is cancer (heuristic) | no |
Also known as: schizophrenia 13 · schizophrenia susceptibility locus, chromosome 15Q13-q14-related · schizophrenia, susceptibility to, 13 · SCZD13
Disease family
This is a subtype of schizophrenia, susceptibility to. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease susceptibility › inherited disease susceptibility › schizophrenia, susceptibility to › schizophrenia 13
Related subtypes (5): schizophrenia 4, schizophrenia 6, schizophrenia 9, schizophrenia 14, schizophrenia 18
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.