01
ABCA4
No data
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Ewing Sarcoma
- Standard Disease Name
- ewing sarcoma
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 612219
- UMLS ID
- C0553580|C3489398|C0877849
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NICHD_1602D:A malignant neoplasm of the bone, or the soft tissue adjacent to bone, that is comprised of primitive neuroectodermal cells.|NCI2016_NCI-GLOSS_1602D:A type of cancer that forms in bone or soft tissue.|NCI2016_02D:A small round cell tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing sarcoma/peripheral neuroectodermal tumor. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms.|MSH2017_2016_08_12: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.|HPO2016_07_04:A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. [HPO:probinson, pmid:17272319]|CSP2006:malignant tumor of bones which always arises in medullary tissue, occurring more often in cylindrical bones, with pain, fever, and leukocytosis.
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Related Targets
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