ORPHA:71274
Disseminated peritoneal leiomyomatosis
Synonyms: DPL · Diffuse peritoneal leiomyomatosis · LPD · Leiomyomatosis peritonealis disseminate
- Type
- Disease
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- Adult
- Status
- active
Disseminated peritoneal leiomyomatosis (DPL) is characterized by the proliferation of multiple benign smooth muscle cell-containing nodules in the peritoneal cavity.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Disseminated peritoneal leiomyomatosis | DPL · Diffuse peritoneal leiomyomatosis · LPD · Leiomyomatosis peritonealis disseminate |
| fr | Léiomyomatose péritonéale disséminée | Léiomyomatose péritonéale diffuse |
| de | Peritoneale Leiomyomatose, disseminierte | DPL · LPD · Peritoneale Leiomyomatose, diffuse |
| es | Leiomiomatosis peritoneal diseminada | LPD · Leiomiomatosis peritoneal difusa |
| it | Leiomiomatosi peritoneale disseminata | DPL · LPD · Leiomiomatosi peritoneale diffusa |
| nl | Gedissemineerde peritoneale leiomyomatose | DPL · Diffuse peritoneale leiomyomatose · LPD · Leiomyomatosis peritonealis disseminata |
| pt | Leiomiomatose peritoneal disseminada | |
| pl | Rozsiana zaotrzewnowa leiomiomatoza | Dpl · Leiomyomatosis peritonealis disseminate · LPD · Rozlana zaotrzewnowa leiomiomatoza |
| cs | Diseminovaná peritoneální leiomyomatóza | DPL · Difuzní peritoneální leiomyomatóza · LPD |
| uk | Дисемінований перитонеальний лейоміоматоз | Дифузний перитонеальний лейоміоматоз · DPL · Дисемінований лейоміоматоз очеревини · LPD |
| zh | 播散性腹膜平滑肌瘤病 | 播散性腹膜平滑肌瘤病 |
| tr | Yaygın peritoneal leiomiyomatoz | DPL · LPD · Yaygın peritoneal leiomyomatoz · Leiyomyomatozis peritonealis disseminate |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D20.1 | NTBT | attributed | validated |
| ICD-11 | 2F7C | NTBT | attributed | validated |
| ICD-11 | XH8MR2 | E | specific | validated |
| MONDO | 0006183 | E | validated | |
| UMLS | C0267785 | E | validated | |
| GARD | 12843 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:676030Primary benign peritoneal tumor
rare abdominal surgical diseases; rare neoplastic diseases - ORPHA:506216Rare disorder potentially indicated for bowel transplant
rare transplant-related disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 150 cases | Worldwide | Case(s) | Validated | [EXPERT] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 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.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/71274
- This record as JSON: /data/d/71274.json