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PedAM

Pediatric Disease Annotations & Medicines



   chondrosarcoma, extraskeletal myxoid
  

Disease ID 1970
Disease chondrosarcoma, extraskeletal myxoid
Definition
A rare malignant soft tissue neoplasm of uncertain differentiation, characterized by the presence of chondroblast-like cells in a myxoid stroma and a multinodular growth pattern. The most common sites of involvement are the deep soft tissues of the extremities, particularly the thigh. It usually presents as an enlarging soft tissue mass. Patients may have long survivals, but local recurrences and metastases occur in approximately half of the cases. The most common site of metastasis is the lungs.
Synonym
chondroid sarcoma
emc
extraosseous chondrosarcoma
extraskeletal chondrosarcoma
extraskeletal myxoid chondrosarcoma
extraskeletal myxoid chondrosarcoma (disorder)
myxoid extraosseous chondrosarcoma
myxoid extraskeletal chondrosarcoma
Orphanet
OMIM
DOID
UMLS
C1275278
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:1)
C0024454  |  maffucci syndrome  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:5)
EWSR1  |  2130  |  ORPHANET
TFG  |  10342  |  CTD_human;ORPHANET
NR4A3  |  8013  |  CTD_human;ORPHANET
TCF12  |  6938  |  ORPHANET
TAF15  |  8148  |  CTD_human;ORPHANET
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1970
Disease chondrosarcoma, extraskeletal myxoid
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype(Waiting for update.)
Disease ID 1970
Disease chondrosarcoma, extraskeletal myxoid
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
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All Snps(Total Genotypes:0)
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GWASdb Annotation(Total Genotypes:0)
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GWASdb Snp Trait(Total Genotypes:0)
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Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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Chemical(Total Drugs:0)
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FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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