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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Retinoblastoma
equivalentClass
Has_NICHD_Parent
Concept_In_Subset
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Retinoblastoma
UMLS_CUI
  • C0035335
Contributing_Source
  • CDISC
  • CTEP
  • NICHD
ALT_DEFINITION
  • Cancer that forms in the tissues of the retina (the light-sensitive layers of nerve tissue at the back of the eye). Retinoblastoma usually occurs in children younger than 5 years. It may be hereditary or nonhereditary (sporadic).NCI-GLOSS
  • A malignant neoplasm originating in the nuclear layer of the retina.CDISC
ICD-O-3_Code
  • 9510/3
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • Retinoblastoma
FULL_SYN
  • RBABNCI
  • RetinoblastomaPTCTEP10038918
  • RetinoblastomaPTNCI
  • RETINOBLASTOMA, MALIGNANTPTCDISC
  • RBSYCDISC
  • RetinoblastomaPTNICHD
  • retinoblastomaPTNCI-GLOSSCDR0000046774
DEFINITION
  • A malignant tumor that originates in the nuclear layer of the retina. As the most common primary tumor of the eye in children, retinoblastoma is still relatively uncommon, accounting for only 1% of all malignant tumors in pediatric patients. These tumors may be multifocal, bilateral, congenital, inherited, or acquired. Seventy-five percent of retinoblastomas are unilateral; 60% occur sporadically. A predisposition to retinoblastoma has been associated with 13q14 cytogenetic abnormalities. Patients with the inherited form also appear to be at increased risk for secondary nonocular malignancies such as osteosarcoma, malignant fibrous histiocytoma, and fibrosarcoma.NCI
code
  • C7541
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