ORPHA:183731
Rare genetic gynecological and obstetrical diseases
- 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 | Rare genetic gynecological and obstetrical diseases | |
| fr | Maladies gynéco-obstétriques rares d'origine génétique | |
| de | Gynäkologische oder geburtshilfliche Krankheit, seltene, genetisch bedingte | |
| es | Enfermedades gineco-obstétricas genéticas raras | |
| it | Malattie genetiche rare ginecologiche e ostetriche | |
| nl | Zeldzame genetische gynaecologische en obstetrische ziektes | |
| pt | Doenças obstétricas e ginecológicas genéticas, raras | |
| pl | Rzadka genetyczna choroba ginekologiczna i położnicza | |
| cs | Vzácná dědičná gynekologicko-porodnická onemocnění | |
| uk | Рідкісні генетично обумовлені гінекологічні та акушерські захворювання | |
| zh | 罕见遗传性妇产科疾病 | |
| tr | Nadir görülen genetik jinekolojik ve obstetrik hastalıklar |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15980 | E | validated | |
| UMLS | C5680528 | 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:98053Rare genetic disease
rare genetic diseases
Children (7):
- ORPHA:202940Anomaly of puberty or/and menstrual cycle of genetic origin
- ORPHA:325665Genetic difference of sex development of gynecological interest
- ORPHA:145Hereditary breast and/or ovarian cancer syndrome
- ORPHA:180188Isolated congenital breast hypoplasia/aplasia
- ORPHA:238744Mammary-digital-nail syndrome
- ORPHA:73217Müllerian aplasia
- ORPHA:64739Ovarian hyperstimulation syndrome
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/183731
- This record as JSON: /data/d/183731.json