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
..expandOsteosarcoma, Juxtacortical (D018217)

       Child Nodes:



 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:8447
Name:Osteosarcoma, Juxtacortical
Definition:A form of osteogenic sarcoma of relatively low malignancy, probably arising from the periosteum and initially involving cortical bone and adjacent connective tissue. It occurs in middle-aged as well as young adults and most commonly affects the lower part of the femoral shaft. (Stedman, 25th ed)
Alternative IDs:
ParentIDs:MESH:D012516
TreeNumbers:C04.557.450.565.575.650.655 |C04.557.450.795.620.655
Synonyms:Juxtacortical Osteosarcoma |Juxtacortical Osteosarcomas |Osteosarcomas, Juxtacortical
Slim Mappings:Cancer
Reference: MedGen: D018217
MeSH: D018217
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants