Osteogenic sarcoma

Preferred Label : Osteogenic sarcoma;

CISMeF acronym : OSRC;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Osteosarcoma; OSRC;

Inheritance : Somatic mutation;

Molecular basis : Susceptibility conferred by mutation in the homolog of the S. pombe checkpoint kinase 2 gene (CHECK2, 604373.0005); Susceptibility conferred by mutation in the tumor protein 53 gene (TP53, 191170.0013);

Neoplasia : Osteogenic sarcoma;

Prefixed ID : #259500;

Details

Origin ID

259500;

UMLS CUI

C0029463;

Automatic exact mappings (from CISMeF team)
- Childhood Osteosarcoma [NCIt concept]
- NCI CTEP SDC Osteosarcoma Sub-Category Terminology [NCIt concept]
- Osteosarcoma NOS [ICD-9 code]
- Osteosarcoma, primary site [ICD-11 Category]
- bone cancer [MedlinePlus Topic]
- malignant neoplasm musculoskeletal [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Osteogenic sarcoma [MedDRA LLT]
- Osteosarcoma [PASCAL descriptor]
- Osteosarcoma [HPO term]
- Osteosarcoma [MedDRA Preferred Term]
- Osteosarcoma [NCIt concept]
- Osteosarcoma [ORDO Disease]
- Osteosarcoma NOS [MedDRA LLT]
- Osteosarcoma of bone (disorder) [SNOMED CT concept]
- Osteosarcoma, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [SNOMED CT concept]
- Sarcoma osteogenic [MedDRA LLT]
- osteosarcoma [DO Concept]
- osteosarcoma [MeSH Descriptor]
- osteosarcoma [MeSH concept]
- osteosarcoma [Radlex concept]
- osteosarcoma, nos [SNOMED Notion]
DO Cross reference
- osteosarcoma [DO Concept]
Genes related to phenotype
- Checkpoint kinase 2 [OMIM gene]
- Rb transcriptional corepressor 1 [OMIM gene]
- Tumor protein p53 [OMIM gene]
HPO term(s)
- Osteosarcoma [HPO term]
- Retinoblastoma [HPO term]
- Somatic mutation [HPO term]
ORDO concept(s)
- Osteosarcoma [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Osteogenic sarcoma [MedDRA LLT]
- Osteosarcoma [MedDRA Preferred Term]
- Osteosarcoma [ORDO Disease]
- Osteosarcoma [NCIt concept]
- Osteosarcoma [HPO term]
- Osteosarcoma (morphologic abnormality) [SNOMED CT concept]
- Osteosarcoma NOS [MedDRA LLT]
- Osteosarcoma, NOS [ICD-O code]
- Osteosarcoma, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [SNOMED CT concept]
- Sarcoma osteogenic [MedDRA LLT]
- osteosarcoma [MeSH Descriptor]
- osteosarcoma [MeSH concept]
- osteosarcoma [Radlex concept]
- osteosarcoma, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients