Low-flow priapism
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare urogenital condition characterized by a persistent unwanted painful erection that lasts more than 4 hours, caused by obstruction of the normal drainage of blood from the erectile tissues, leading to ischemia. It may be due to hematological diseases, metabolic or neurological disorders, and some erectile dysfunction medications. If the condition continues for several days, abnormal thickening and scarring of the erectile tissue may develop, causing permanent erectile dysfunction.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Low-flow priapism | |
| fr | Priapisme à flux réduit | |
| de | Priapismus, Low-Flow-Typ | |
| es | Priapismo de bajo flujo | |
| it | Priapismo a basso flusso | |
| nl | Low-flow priapisme | |
| pt | Priapismo de baixo fluxo | |
| pl | Priapizm niskoprzepływowy | |
| cs | Nízkoprůtokový priapismus | |
| uk | Ішемічний пріапізм | |
| zh | 低血流阴茎异常勃起 | |
| tr | Düşük akışlı priapizm |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | N48.3 | NTBT | attributed | validated |
| ICD-11 | GB06.1 | NTBT | index | validated |
| MONDO | 0004745 | E | validated | |
| MONDO | 4745 | E | validated | |
| UMLS | C2711256 | E | validated | |
| GARD | 19933 | 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:101433Rare urogenital disease
rare urogenital 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 | — | Europe | Class only | Validated | European Medicines Agency 2010[OTHER] |
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/140949
- This record as JSON: /data/d/140949.json