Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Retinoblastoma

Synonyms

Retinal Glioblastomas

Definitions

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)

ID

http://purl.bioontology.org/ontology/MESH/D012175

altLabel

Retinal Glioblastomas

Retinoblastomas

Retinoblastoma, Hereditary

Retinal Neuroblastomas

Hereditary Retinoblastomas

Retinal Gliomas

Retinal Neuroblastoma

Neuroblastomas, Retinal

Cancer, Retinoblastoma Eye

Familial Retinoblastoma

Retinoblastoma Eye Cancers

Cancers, Retinoblastoma Eye

Sporadic Retinoblastomas

Glioblastomas, Retinal

Retinal Glioblastoma

Eye Cancer, Retinoblastoma

Eye Cancers, Retinoblastoma

Retinoblastoma, Sporadic

Gliomas, Retinal

Retinoblastoma Eye Cancer

Neuroblastoma, Retinal

Retinoblastomas, Familial

Retinoblastomas, Sporadic

Sporadic Retinoblastoma

Retinal Glioma

Familial Retinoblastomas

Retinoblastomas, Hereditary

Retinoblastoma, Familial

Glioblastoma, Retinal

Hereditary Retinoblastoma

Glioma, Retinal

AN

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

AQL

BL BS CF CH CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SC SU TH UL UR VE VI

cui

C0751483

C0751484

C0035335

DC

1

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)

DX

19660101

FX

D016161

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000737

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000556

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000648

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000098

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Inverse of RO

http://purl.bioontology.org/ontology/MESH/D019572

http://purl.bioontology.org/ontology/MESH/D016161

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D012162

http://purl.bioontology.org/ontology/MESH/D057130

http://purl.bioontology.org/ontology/MESH/D015418

http://purl.bioontology.org/ontology/MESH/D003317

http://purl.bioontology.org/ontology/MESH/D000077765

http://purl.bioontology.org/ontology/MESH/D015792

http://purl.bioontology.org/ontology/MESH/D000417

http://purl.bioontology.org/ontology/MESH/D056846

http://purl.bioontology.org/ontology/MESH/D000071700

http://purl.bioontology.org/ontology/MESH/D005910

http://purl.bioontology.org/ontology/MESH/D015794

http://purl.bioontology.org/ontology/MESH/D003103

http://purl.bioontology.org/ontology/MESH/D015799

http://purl.bioontology.org/ontology/MESH/D005729

http://purl.bioontology.org/ontology/MESH/D018306

http://purl.bioontology.org/ontology/MESH/D058540

http://purl.bioontology.org/ontology/MESH/D058494

http://purl.bioontology.org/ontology/MESH/D049970

http://purl.bioontology.org/ontology/MESH/D004370

http://purl.bioontology.org/ontology/MESH/D015783

http://purl.bioontology.org/ontology/MESH/D010871

http://purl.bioontology.org/ontology/MESH/D012174

http://purl.bioontology.org/ontology/MESH/D018242

Mapped from

http://purl.bioontology.org/ontology/MESH/C566714

MDA

19990101

MMR

20180615

MN

C04.557.465.625.600.725

C11.270.862

C04.557.470.670.725

C04.557.580.625.600.725

C11.319.475.760

C04.588.364.818.760

C11.768.717.760

notation

D012175

prefLabel

Retinoblastoma

TERMUI

T036237

T036235

T371983

T371985

T371984

T036236

T727501

T036238

TH

NLM (1998)

NLM (2011)

NLM (2000)

NLM (1966)

ORD (2010)

GHR (2014)

tui

T191

subClassOf

http://purl.bioontology.org/ontology/MESH/D015785

http://purl.bioontology.org/ontology/MESH/D019572

http://purl.bioontology.org/ontology/MESH/D018302

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http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7541 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/OMIM/614041 Online Mendelian Inheritance in Man CUI
http://purl.obolibrary.org/obo/DOID_768 Cell Line Ontology Subset for Chinese National Infrastructure of Cell Line Resource (NICR) LOOM
http://purl.obolibrary.org/obo/DOID_768 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/LNC/LA16305-7 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/LNC/LA16305-7 Logical Observation Identifier Names and Codes LOOM
http://purl.bioontology.org/ontology/OMIM/180200 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/180200 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU034783 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/MTHU034783 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0035335 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0035335 MedlinePlus Health Topics LOOM
http://purl.obolibrary.org/obo/NCIT_C7541 Human Phenotype Ontology China LOOM
http://purl.bmicc.cn/ontology/ICD11CN/2D02.2 International Classification of Diseases, 11th Edition, China LOOM
http://purl.obolibrary.org/obo/MPATH_378 Human Phenotype Ontology China LOOM