Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C7541> ?p ?o ?g. }
- NCIT_C7541 IAO_0000115 "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. Approximately 95% of cases are diagnosed before age 5. 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." @default.
- NCIT_C7541 NCIT_A14 NCIT_C9292 @default.
- NCIT_C7541 NCIT_A32 NCIT_C176985 @default.
- NCIT_C7541 NCIT_A32 NCIT_C177621 @default.
- NCIT_C7541 NCIT_NHC0 "C7541" @default.
- NCIT_C7541 NCIT_P106 "Neoplastic Process" @default.
- NCIT_C7541 NCIT_P107 "Retinoblastoma" @default.
- NCIT_C7541 NCIT_P108 "Retinoblastoma" @default.
- NCIT_C7541 NCIT_P207 "C0035335" @default.
- NCIT_C7541 NCIT_P322 "CDISC" @default.
- NCIT_C7541 NCIT_P322 "CPTAC" @default.
- NCIT_C7541 NCIT_P322 "CTEP" @default.
- NCIT_C7541 NCIT_P322 "CTRP" @default.
- NCIT_C7541 NCIT_P322 "Cellosaurus" @default.
- NCIT_C7541 NCIT_P322 "GDC" @default.
- NCIT_C7541 NCIT_P322 "MedDRA" @default.
- NCIT_C7541 NCIT_P322 "NICHD" @default.
- NCIT_C7541 NCIT_P322 "PCDC" @default.
- NCIT_C7541 NCIT_P325 "A malignant neoplasm originating in the nuclear layer of the retina." @default.
- NCIT_C7541 NCIT_P325 "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. Approximately 95% of cases are diagnosed before age 5. 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." @default.
- NCIT_C7541 NCIT_P325 "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)." @default.
- NCIT_C7541 NCIT_P334 "9510/3" @default.
- NCIT_C7541 NCIT_P363 "Malignant" @default.
- NCIT_C7541 NCIT_P366 "Retinoblastoma" @default.
- NCIT_C7541 NCIT_P375 "9510/3" @default.
- NCIT_C7541 NCIT_P375 "Retinoblastoma" @default.
- NCIT_C7541 NCIT_P375 "Retinoblastoma, NOS" @default.
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