raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3394

Soft tissue sarcoma

Synonyms: Malignant mesenchymal tumor · Malignant soft tissue tumor · Soft part sarcoma

Type
Clinical group
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
LangNameSynonyms
enSoft tissue sarcomaMalignant mesenchymal tumor · Malignant soft tissue tumor · Soft part sarcoma
frSarcome des tissus mousSarcome des parties molles · Tumeur maligne des parties molles · Tumeur maligne des tissus mous · Tumeur mésenchymateuse maligne
deWeichteilsarkomMesenchymaler Tumor, maligner · Weichteiltumor, maligner
esSarcoma de partes blandasSarcoma de tejidos blandos · Tumor maligno de tejidos blandos · Tumor mesenquimal maligno
itSarcoma dei tessuti molliSarcoma delle parti molli · Tumore maligno dei tessuti molli · Tumore mesenchimale maligno
nlWekedelensarcoomKwaadaardige wekedelentumor · Maligne mesenchymale tumor · Maligne wekedelentumor
ptSarcoma de tecidos molesTumor mesenquimatoso maligno
plMięsak tkanek miękkichZłośliwy guz mezenchymalny · Złośliwy guz tkanek miękkich
csSarkom měkkých tkáníMaligní mezenchymový nádor · Maligní nádor měkkých tkání
ukСаркома мяких тканинЗлоякісна мезенхімальна пухлина · Злоякісна пухлина мяких тканин · Саркома мяких тканин
zh软组织肉瘤恶性软组织肿瘤
trYumuşak doku sarkomuYumuşak bölüm sarkomu · Habis mezenkimal tümör · Habis yumuşak doku tümörü
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0018078Evalidated
MONDO18078Evalidated
GARD4898Evalidated
MedDRA10075333Evalidated

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):

Children (26):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

3 records
TypeClassValueAreaQualificationValidationSource
Annual incidence1-9 / 100 0003.6 / 100 000FranceValue and classValidated21826194[PMID]
Point prevalence1-5 / 10 00030 / 100 000EuropeValue and classValidatedEuropean Medicines Agency 2015[OTHER]
Annual incidence1-9 / 100 0004.74 / 100 000EuropeValue and classValidatedRARECARE surveillance of rare cancers in Europe[OTHER]

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