Liposarcoma

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 8
OrphanetNr: 69078
OMIM Id: 613488
ICD-10: C49
UMLs: C0023827
MeSH: D008080
MedDRA: 10024627
Snomed: 254829001
49430005

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Unknown
[Orphanet]
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Soft tissue sarcoma
 -Rare oncologic disease

Symptom Information: Sort by abundance 

1
(HPO:0011277) Abnormality of the urinary system physiology Occasional [Orphanet] 5 / 7739
2
(HPO:0002027) Abdominal pain Occasional [Orphanet] 184 / 7739
3
(HPO:0001031) Subcutaneous lipoma Very frequent [Orphanet] 112 / 7739
4
(HPO:0100526) Neoplasm of the lung Occasional [Orphanet] 26 / 7739
5
(HPO:0012268) Myxoid liposarcoma 1 / 7739
6
(HPO:0030448) Soft tissue sarcoma Very frequent [Orphanet] 18 / 7739
7
(HPO:0001428) Somatic mutation 100 / 7739
8
(HPO:0012719) Functional abnormality of the gastrointestinal tract Occasional [Orphanet] 17 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Description: (OMIM) Myxoid liposarcoma is a soft tissue tumor that tends to occur in the limbs (especially the thigh) of patients ranging in age from 35 to 55 years. It is defined by the presence of a hypocellular spindle cell ...