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Diseases

Sarcoma, Synovial

sarcoma, synovial

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Sarcoma, Synovial
Standard Disease Name
sarcoma, synovial
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D013584
OMIM ID
300813
UMLS ID
C0039101
HPO ID
No data

Description and Extensions

Description
NCI2016_NCI-GLOSS_1602D:A malignant tumor that develops in the synovial membrane of the joints.|NCI2016_CDISC_1602D:A malignant neoplasm that usually arises in the synovial membranes of the joints and the synovial cells of the tendons and bursae.|NCI2016_02D:A malignant neoplasm characterized by the chromosomal translocation t(X;18)(p11;q11). It can occur at any age, but mainly affects young adults, more commonly males. Although any site can be affected, the vast majority of the cases arise in the deep soft tissues of extremities, especially around the knee. Microscopically, synovial sarcoma is classified as monophasic (with a spindle or epithelial cell component) or biphasic (with both spindle and epithelial cell components). Synovial sarcomas can recur or metastasize to the lungs, bones, and lymph nodes.|MSH2017_2016_08_12:A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363)|HPO2016_07_04:A type of mesenchymal tissue cell tumor that exhibits epithelial differentiation, which most frequently arises in the extremities. [HPO:probinson]
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
ABCC6
ATP binding cassette subfamily C member 6
ATP binding cassette subfamily C member 6
05
AKR1B1
aldo-keto reductase family 1 member B
aldo-keto reductase family 1 member B
06
AKR1C1
aldo-keto reductase family 1 member C1
aldo-keto reductase family 1 member C1
07
AKR1C2
aldo-keto reductase family 1 member C2
aldo-keto reductase family 1 member C2
08
AKR1C3
aldo-keto reductase family 1 member C3
aldo-keto reductase family 1 member C3