Osteosarcoma

Symptom Information:

Symptom ID: HPO:0002669
Synonyms:
Osteogenic sarcoma [HPO:0002669]
Osteogenic sarcoma [OMIM:Osteogenic sarcoma]
Osteosarcoma [OMIM:Osteosarcoma]
Osteosarcomas [OMIM:Osteosarcomas]
Osteosarcoma [MedDRA:10031291]
Quality:
Cross references:
OMIM: "Osteogenic sarcoma" [OMIM:Osteogenic sarcoma]
OMIM: "Osteosarcoma" [OMIM:Osteosarcoma]
OMIM: "Osteosarcomas" [OMIM:Osteosarcomas]
Is a (Direct Parents):
MedDRA Malignant musculoskeletal and connective tissue neoplasms
HPO         Sarcoma
HPO         Neoplasm of the skeletal system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Neoplasm of the skeletal system(HPO:0010622)
                Osteosarcoma(HPO:0002669)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skeletal system(HPO:0010622)
                Osteosarcoma(HPO:0002669)
          Neoplasm by histology(HPO:0011792)
             Sarcoma(HPO:0100242)
                Osteosarcoma(HPO:0002669)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue neoplasms(MedDRA:10028389)
       Malignant musculoskeletal and connective tissue neoplasms(MedDRA:10025681)
          Osteosarcoma(HPO:0002669)
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Blackfan-Diamond anemia (Orphanet:124)
DIAMOND-BLACKFAN ANEMIA 1 (OMIM:105650)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
LI-FRAUMENI SYNDROME 1 (OMIM:151623)
Li-Fraumeni syndrome (Orphanet:524)
OSLAM syndrome (Orphanet:2760)
Osteosarcoma (Orphanet:668)
PAGET DISEASE OF BONE 1 (OMIM:167250)
PREMATURE AGING SYNDROME, OKAMOTO TYPE (OMIM:601811)
Retinoblastoma (Orphanet:790)
Rothmund-Thomson syndrome (Orphanet:2909)
Werner syndrome (Orphanet:902)