retinoblastoma

Preferred Label : retinoblastoma;

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 synonym : retinoblastomas; retinal neuroblastoma; retinal glioma; glioblastoma, retinal; retinal glioblastoma; retinal glioblastomas; glioma, retinal; gliomas, retinal; retinal gliomas; neuroblastoma, retinal; neuroblastomas, retinal; retinal neuroblastomas; glioblastomas, retinal; eye cancer, retinoblastoma; Cancer, Retinoblastoma Eye; Cancers, Retinoblastoma Eye; Eye Cancers, Retinoblastoma; Retinoblastoma Eye Cancer; Retinoblastoma Eye Cancers;

MeSH hyponym : familial retinoblastoma; sporadic retinoblastoma; Retinoblastoma, Sporadic; Retinoblastomas, Sporadic; Sporadic Retinoblastomas; Familial Retinoblastomas; Retinoblastoma, Familial; Retinoblastomas, Familial; Hereditary Retinoblastoma; Hereditary Retinoblastomas; Retinoblastoma, Hereditary; Retinoblastomas, Hereditary;

MeSH annotation : coordinate IM with RETINAL NEOPLASMS (IM); /genetics: consider also GENES, RETINOBLASTOMA;

Wikipedia link : https://en.wikipedia.org/wiki/Retinoblastoma;

Details

Origin ID

D012175;

UMLS CUI

C0035335;

Allowable qualifiers
- blood [MeSH Qualifier]
- blood supply [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- chemistry [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- secondary [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- ultrastructure [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Hereditary Retinoblastoma [NCIt concept]
- Hereditary retinoblastoma [ORDO Disease]
- NCI CTEP SDC Retinoblastoma Sub-Category Terminology [NCIt concept]
- Rat Retinoblastoma [NCIt concept]
- Retinal Neuroblastoma [NCIt concept]
- Retinoblastoma [ACR pathology]
- Retinoblastoma NOS [ICD-9 code]
- Retinoblastoma-Associated Protein [NCIt concept]
- Rubidium [NCIt concept]
- Sporadic Retinoblastoma [NCIt concept]
- eye cancer [MedlinePlus Topic]
- familial retinoblastoma [DO Concept]
Currated CISMeF NLP mapping
- RETINOBLASTOMA [WHO-ART Preferred Term]
- Retinoblastoma [PASCAL descriptor]
- Retinoblastoma [MedDRA Preferred Term]
- Retinoblastoma [ICD-11 Subcategory]
- Retinoblastoma [NCIt concept]
- Retinoblastoma [OMIM Phenotype]
- Retinoblastoma [HPO term]
- Retinoblastoma [ORDO Disease]
- Retinoblastoma [HRDO Sign]
- Retinoblastoma (disorder) [SNOMED CT concept]
- Retinoblastoma (morphologic abnormality) [SNOMED CT concept]
- Retinoblastoma NOS [MedDRA LLT]
- Retinoblastoma, NOS [ICD-O code]
- retinoblastoma [DO Concept]
- retinoblastoma [Disease (Nov.)]
- retinoblastoma [Radlex concept]
- retinoblastoma, nos [SNOMED Notion]
DO Cross reference
- familial retinoblastoma [DO Concept]
- retinoblastoma [DO Concept]
HPO term
- Retinoblastoma [HPO term]
Indexing information
- LCP1 protein, human [MeSH Supplementary Concept]
- RBBP9 protein, human [MeSH Supplementary Concept]
- Rbbp9 protein, mouse [MeSH Supplementary Concept]
- Rbbp9 protein, rat [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Genetic eye tumor [ORDO Disease]
- Genetic vitreous-retinal disease [ORDO Disease]
- Rare eye tumor [ORDO Disease]
- Rare genetic tumor [ORDO Disease]
MedlinePlus topic(s)
- eye cancer [MedlinePlus Topic]
ORDO relation(s)
- Retinoblastoma [ORDO Disease]
Record concept(s)
- familial retinoblastoma [MeSH concept]
- retinoblastoma [MeSH concept]
- sporadic retinoblastoma [MeSH concept]
Related MeSH Supplementary Concept(s)
- osteosarcoma, Retinoblastoma-Related [MeSH Supplementary Concept]
See also
- genes, retinoblastoma [MeSH Descriptor]
- retinal neoplasms [MeSH Descriptor]
See also (suggested by CISMeF)
- neuroblastoma [MeSH Descriptor]
- retinoblastoma protein [MeSH Descriptor]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- RETINOBLASTOMA [WHO-ART Preferred Term]
- Retinal Neuroblastoma [NCIt concept]
- Retinoblastoma [ORDO Disease]
- Retinoblastoma [MedDRA Preferred Term]
- Retinoblastoma [HPO term]
- Retinoblastoma [OMIM Phenotype]
- Retinoblastoma [HRDO Sign]
- Retinoblastoma [PASCAL descriptor]
- Retinoblastoma [NCIt concept]
- Retinoblastoma (disorder) [SNOMED CT concept]
- Retinoblastoma (morphologic abnormality) [SNOMED CT concept]
- Retinoblastoma NOS [MedDRA LLT]
- Retinoblastoma, NOS [ICD-O code]
- retinoblastoma [Radlex concept]
- retinoblastoma [DO Concept]
- retinoblastoma [Disease (Nov.)]
- retinoblastoma, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- familial retinoblastoma [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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