ORPHA:180208
Anomaly of puberty or/and menstrual cycle
- Type
- Category
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Anomaly of puberty or/and menstrual cycle | |
| fr | Anomalie du cycle menstruel et/ou de la puberté | |
| de | Störungen der Pubertät und/oder der Menstruation | |
| es | Anomalía de la pubertad y/o del ciclo menstrual | |
| it | Anomalia della pubertà e/o del ciclo mestruale | |
| nl | Anomalie van puberteit of/en menstruatiecyclus | |
| pt | Anomalia da puberdade e/ou do ciclo menstrual | |
| pl | Zaburzenia dojrzewania i/lub cyklu menstruacyjnego | |
| cs | Poruchy pohlavního dospívání a/nebo menstruačního cyklu | |
| uk | Аномалія статевого дозрівання та/або менструального циклу | |
| zh | 青春期或/和月经周期异常 | |
| tr | Ergenlik ve / veya adet döngüsü anormalliği |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15860 | E | validated | |
| UMLS | C5680481 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:96344Rare gynecologic or obstetric disease
rare gynecological and obstetric diseases
Children (7):
- ORPHA:174590Congenital hypogonadotropic hypogonadism
- ORPHA:785Estrogen resistance syndrome
- ORPHA:168588Hyperandrogenism due to cortisone reductase deficiency
- ORPHA:498251Menstrual cycle-dependent periodic fever
- ORPHA:95709Rare acquired premature ovarian failure
- ORPHA:95710Rare non-acquired premature ovarian failure
- ORPHA:435561Rare precocious puberty in female
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180208
- This record as JSON: /data/d/180208.json