Gestational trophoblastic neoplasm
Synonyms: GTN
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare, malignant group of gestational trophoblastic diseases always following pregnancy, most often molar pregnancy (hydatidiform mole). Four histological forms are described: invasive mole, gestational choriocarcinoma, placental site trophoblastic tumor (PSTT) and epithelioid trophoblastic tumor (ETT).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Gestational trophoblastic neoplasm | GTN |
| fr | Tumeur trophoblastique gestationnelle | TTG |
| de | Neoplasie, gestationsbedingte trophoblastische | Schwangerschafts-Trophoblastentumor |
| es | Neoplasia trofoblástica gestacional | NTG |
| it | Tumore trofoblastico della gravidanza | = en |
| nl | Gestationeel trofoblastisch neoplasma | GTN · Gestationele trofoblasttumor |
| pt | Neoplasia trofoblástica gestacional | = en |
| pl | Ciążowy nowotwór trofoblastyczny | = en |
| cs | Gestační trofoblastická neoplázie | = en |
| uk | Гестаційне трофобластичне новоутворення | = en |
| zh | 妊娠滋养细胞肿瘤 | = en |
| tr | Gestasyonel trofoblastik neoplazm | = en |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 2C75.0 | E | specific | validated |
| MONDO | 0018944 | E | validated | |
| MONDO | 18944 | E | validated | |
| UMLS | C1135868 | E | validated | |
| GARD | 6498 | E | validated | |
| MedDRA | 10061988 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:254685Gestational trophoblastic disease
rare neoplastic diseases; rare gynecological and obstetric diseases
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
| Annual incidence | Unknown | — | 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/59305
- This record as JSON: /data/d/59305.json