Postpartum psychosis
diseaseOn this page
Also known as puerperal psychosis
Summary
Postpartum psychosis (MONDO:0018623) is a disease and 4 clinical trials. Top therapeutic interventions include brexanolone. A subtype of psychotic disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: 1-9 / 100 000 (Worldwide) [Orphanet-validated]
- Clinical trials: 4
Clinical features
Epidemiology
Prevalence records
1 prevalence record(s), Orphanet:
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 4 | Worldwide | Validated |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | postpartum psychosis |
| Mondo ID | MONDO:0018623 |
| Orphanet | 443173 |
| ICD-10-CM | F53, F53.1 |
| SNOMED CT | 18260003 |
| UMLS | C0520678 |
| MedGen | 636162 |
| GARD | 0021853 |
| Is cancer (heuristic) | no |
Also known as: puerperal psychosis
Disease family
This is a subtype of psychotic disorder. 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 › human disease › disease by developmental or physiological process › psychiatric disorder › cognitive disorder › psychotic disorder › postpartum psychosis
Related subtypes (7): schizophreniform disorder, alcoholic psychosis, delusional disorder, substance-induced psychosis, schizophrenia, methamphetamine-induced psychosis, schizoaffective disorder
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: 4.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 3 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05314153 | EARLY_PHASE1 | COMPLETED | Effects Zulresso on Postpartum Psychosis |
| NCT01172106 | Not specified | UNKNOWN | Impact of Family Psychoeducation on Psychosis |
| NCT02661789 | Not specified | COMPLETED | Neuropsychobiological Correlates of Sex-steroid Hormone Manipulation in Healthy Women: a Risk Model for Depression |
| NCT03615794 | Not specified | COMPLETED | A Study of Pregnant and Postpartum Women With and Without Mood Disorders |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| BREXANOLONE | 4 | 1 |
Related Atlas pages
- Drugs: Brexanolone