ORPHA:180068
Partial bilateral aplasia of the Müllerian ducts
Synonyms: Incomplete bilateral aplasia of the Müllerian ducts
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Partial bilateral aplasia of the Müllerian ducts | Incomplete bilateral aplasia of the Müllerian ducts |
| fr | Aplasie bilatérale partielle des canaux de Müller | Aplasie bilatérale incomplète des canaux de Müller |
| de | Aplasie des Müller-Ganges, bilaterale inkomplette | Partielle bilaterale Aplasie des Müllerschen Gangs |
| es | Aplasia bilateral parcial del conducto de Müller | Aplasia bilateral incompleta del conducto de Müller |
| it | Aplasia bilaterale parziale del dotto mülleriano | Aplasia bilaterale incompleta del dotto mülleriano |
| nl | Partiële bilaterale aplasie van gang van Müller | Onvolledige bilaterale aplasie van gang van Müller |
| pt | Aplasia parcial bilateral do ducto mulleriano | |
| pl | Częściowa obustronna aplazja przewodów Müllera | Niecałkowita obustronna aplazja przewodów Müllera |
| cs | Parciální oboustranná aplázie Müllerových vývodů | Nekompletní oboustranná aplázie Müllerových vývodů |
| uk | Часткова двостороння аплазія мюллерових проток | Неповна двостороння аплазія мюллерових проток |
| zh | 双侧苗勒管部分发育不全 | 双侧苗勒管不完全发育 |
| tr | Müllerian kanallarının kısmi bilateral aplazisi | Müllerian kanalların tamamlanmamış bilateral aplazisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015830 | E | validated | |
| MONDO | 15830 | E | validated | |
| UMLS | C5679589 | 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 (1):
- ORPHA:73217Müllerian aplasia
rare developmental anomalies during embryogenesis; rare genetic diseases; rare urogenital diseases; rare gynecological and obstetric diseases; rare transplant-related disorders
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/180068
- This record as JSON: /data/d/180068.json