ORPHA:696830
Female adnexal tumor of probable Wolffian origin
Synonyms: FATWO
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult, Elderly
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Female adnexal tumor of probable Wolffian origin | FATWO |
| fr | Tumeur wolffienne annexielle | = en |
| de | Wolff'scher-Adnextumor | FATWO · Tumor der weiblichen Adnexe mit vermutlichem Ursprung in den Residuen der Wolff'schen Gänge · Wolff-Adnextumor |
| es | Tumor anexial femenino de probable origen wolffiano | FATWO · TAFOW |
| it | Tumore annessiale femminile di probabile origine wolffiana | = en |
| nl | Vrouwelijke tumor van huidadnexen waarschijnlijk ontstaan in gang van Wolff | = en |
| pt | Female Adnexal Tumor of Probable Wolffian Origin | |
| pl | Female adnexal tumor of probable Wolffian origin | = en |
| cs | Female adnexal tumor of probable Wolffian origin | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C57.4 | NTBT | attributed | validated |
| ICD-11 | 2C72.Y | NTBT | attributed | 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:180220Rare uterine adnexal tumor
rare neoplastic diseases; rare gynecological and obstetric diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
| Cases/families | 90 cases | Worldwide | Case(s) | Validated | 30880826[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/696830
- This record as JSON: /data/d/696830.json