raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:213615

Rhabdomyosarcoma of the corpus uteri

Type
Disease
Group
Disorder
Status
active

Rhabdomyosarcoma of the corpus uteri is an extremely rare, highly malignant soft tissue sarcoma located in the uterine body and arising from primitive mesenchymal cells displaying variable degrees of skeletal muscle differentiation. It most often presents with abnormal vaginal discharge or dysfunctional uterine bleeding, abdominal pain and lower abdominal mass. Association with DICER1 syndrome has been reported.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRhabdomyosarcoma of the corpus uteri
frRhabdomyosarcome du corps de l'utérus
deRhabdomyosarkom des Corpus uteri
esRabdomiosarcoma de cuerpo de útero
itRabdomiosarcoma del corpo uterino
nlRhabdomyosarcoom van corpus uteriRhabdomyosarcoom van baarmoederlichaam
ptRabdomiossarcoma do corpo uterino
plMięsak prążkowanokomórkowy trzonu macicy
csRhabdomyosarkom těla děložního
ukРабдоміосаркома тіла матки
zh子宫体横纹肌肉瘤
trKorpus uteri rabdomyosarkomu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C54.2BTNTattributedvalidated
ICD-112B55.YNTBTindexvalidated
MONDO0016260Evalidated
UMLSC4706451Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card