Postpartum psychosis
Synonyms: Puerperal psychosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare gynecologic or obstetric disease characterized by an abrupt onset of psychiatric symptoms during the first weeks after childbirth. Clinical features include mood changes, depression, anxiety, delusions, and hallucinations, among others. The disease is associated with a risk of suicide or infanticide, as well as an increased risk for recurrence after the next pregnancy and future non-pregnancy related psychotic episodes.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Postpartum psychosis | Puerperal psychosis |
| fr | Psychose puerpérale | Psychose du post-partum |
| de | Postpartale Psychose | Wochenbettpsychose |
| es | Psicosis posparto | Psicosis puerperal |
| it | Psicosi postpartum | Psicosi puerperale |
| nl | Postpartumpsychose | Puerperale psychose |
| pt | Psicose pós-parto | |
| pl | Psychoza poporodowa | = en |
| cs | Laktační psychóza | Poporodní psychóza · Puerperální psychóza |
| uk | Післяпологовий психоз | Пологовий психоз |
| zh | 产后精神病 | 产褥期精神病 |
| tr | Doğum sonrası psikoz | Doğum sonrası psikoz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | F53.1 | NTBT | index | validated |
| ICD-11 | 6E21 | NTBT | attributed | validated |
| MONDO | 0018623 | E | validated | |
| UMLS | C0520678 | E | validated | |
| MedDRA | 10006362 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:163637Rare disorder related with pregnancy, childbirth and puerperium
rare gynecological and obstetric diseases - ORPHA:98033Rare neurologic disease with psychiatric involvement
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 4 / 100 000 | Worldwide | Value and class | Validated | 31335024[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/443173
- This record as JSON: /data/d/443173.json