Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandOsteosarcoma (D012516)
..Starting node
..expandSarcoma, Ewing (D012512)

       Child Nodes:
........expandAskin Tumor (C563168)



 Sister Nodes: 
..expandOslam syndrome (C537138)
..expandOsteosarcoma, Juxtacortical (D018217)
..expandOsteosarcoma, Retinoblastoma-Related (C566714)
..expandPremature aging, Okamoto type (C535270)
..expandSarcoma, Ewing (D012512) Child1
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:9984
Name:Sarcoma, Ewing
Definition:A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. The tumor occurs usually before the age of 20, about twice as frequently in males as in females.
Alternative IDs:OMIM:612219
ParentIDs:MESH:D012516
TreeNumbers:C04.557.450.565.575.650.800 |C04.557.450.795.620.800
Synonyms:ASKIN TUMOR, INCLUDED |ES |Ewing Sarcoma |Ewing's Sarcoma |Ewings Sarcoma |Ewing's Tumor |Ewings Tumor |Ewing Tumor |NEUROEPITHELIOMA, PERIPHERAL, INCLUDED |PNE, INCLUDED |Sarcoma, Ewings |Sarcoma, Ewing's |Tumor, Ewing |Tumor, Ewing's
Slim Mappings:Cancer
Reference: MedGen: D012512
MeSH: D012512
OMIM: 612219;

Genes: EWSR1;
Phenotypes
1 HP:0012254Ewing sarcoma
2 HP:0001428Somatic mutation
Disease Causing ClinVar Variants