Postorgasmic illness syndrome
Synonyms: POIS
- Type
- Clinical syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult
- Status
- active
Postorgasmic illness syndrome is a rare urogenital disease characterized by the appearance of flu-like symptoms (fever, extreme fatigue, myalgia, itchy burning eyes, nasal congestion/rhinorrhea), as well as mood changes, irritability and concentration, memory and attention difficulties, within a few minutes to a few hours after ejaculation. Symptoms disappear spontaneously 3-7 days after onset.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Postorgasmic illness syndrome | POIS |
| fr | Maladie postorgasmique | = en |
| de | Postorgasmic-Illness-Syndrom | = en |
| es | Síndrome de enfermedad postorgásmica | = en |
| it | Sindrome post-orgasmica | = en |
| nl | Postorgastische ziekte-syndroom | = en |
| pt | Síndrome de doença pós-orgásmica | = en |
| pl | Zespół choroby postorgazmicznej | = en |
| cs | Postorgasmická nemoc | = en |
| uk | Синдром посторгазмової хвороби | = en |
| zh | 性高潮后疾病综合征 | = en |
| tr | Postorgazmik hastalık sendromu | = en |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | F52.3 | NTBT | attributed | validated |
| ICD-11 | HA02.Y | NTBT | index | validated |
| MONDO | 0017213 | E | validated | |
| UMLS | C4749582 | E | validated | |
| GARD | 10809 | 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 (1):
- ORPHA:182222Rare systemic disease
rare systemic and rheumatological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
| Cases/families | 45 cases | Worldwide | Case(s) | Validated | 21241453[PMID] |
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
18 annotations · validated 2016-10-31| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0011446 | Abnormality of higher mental function | |
| HP:0012378 | Fatigue | |
| Frequent (79-30%) | ||
| HP:0000366 | Abnormality of the nose | |
| HP:0001945 | Fever | |
| HP:0002315 | Headache | |
| HP:0000975 | Hyperhidrosis | |
| HP:0000822 | Hypertension | |
| HP:0000737 | Irritability | |
| Occasional (29-5%) | ||
| HP:0000622 | Blurred vision | |
| HP:0000750 | Delayed speech and language development | |
| HP:0000716 | Depression | |
| HP:0001260 | Dysarthria | |
| HP:0001609 | Hoarse voice | |
| HP:0003552 | Muscle stiffness | |
| HP:0001324 | Muscle weakness | |
| HP:0001962 | Palpitations | |
| HP:0000613 | Photophobia | |
| HP:0000217 | Xerostomia | |
Run the differential on the 2 obligate / very frequent terms
Annotation source: 21241453[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/279947
- This record as JSON: /data/d/279947.json