loading...| Preferred Name | Retinoblastoma [Disease/Finding] | |
| Synonyms |
Eye Cancer, Retinoblastoma Neuroblastoma, Retinal Glioma, Retinal Retinoblastoma Glioblastoma, Retinal |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002615 |
|
| altLabel |
Eye Cancer, Retinoblastoma Neuroblastoma, Retinal Glioma, Retinal Retinoblastoma Glioblastoma, Retinal |
|
| cui |
C0035335 |
|
| May be treated by |
http://purl.bioontology.org/ontology/NDFRT/N0000151706 http://purl.bioontology.org/ontology/NDFRT/N0000151707 http://purl.bioontology.org/ontology/NDFRT/N0000190896 http://purl.bioontology.org/ontology/NDFRT/N0000146314 http://purl.bioontology.org/ontology/NDFRT/N0000190895 http://purl.bioontology.org/ontology/NDFRT/N0000146452 |
|
| 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) |
|
| MESH DUI |
D012175 |
|
| MeSH name |
Retinoblastoma |
|
| MESH UI |
M0018961 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000002615 |
|
| NUI |
N0000002615 |
|
| prefLabel |
Retinoblastoma [Disease/Finding] |
|
| SNOMED CID |
370967009 |
|
| tui |
T191 |
|
| subClassOf |