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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000002615
http://purl.bioontology.org/ontology/NDFRT/N0000002615
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|---|---|
| Preferred Name | Retinoblastoma [Disease/Finding] |
| Synonyms |
Eye Cancer, Retinoblastoma
Neuroblastoma, Retinal
Glioma, Retinal
Retinoblastoma
Glioblastoma, Retinal
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Eye Cancer, Retinoblastoma
Neuroblastoma, Retinal
Glioma, Retinal
Retinoblastoma
Glioblastoma, Retinal
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|---|---|
| prefLabel | Retinoblastoma [Disease/Finding]
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| MESH DEFINITION | A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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| MESH DUI | D012175
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| MESH UI | M0018961
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| MeSH name | Retinoblastoma
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| type | |
| tui | T191
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| SNOMED CID | 370967009
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| May be treated by |
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| notation | N0000002615
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| Semantic type UMLS property | |
| NUI | N0000002615
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| cui | C0035335
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| NDFRT kind | DISEASE_KIND
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| subClassOf |
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