ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Genes, Retinoblastoma

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Inheritance Patterns ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Retinoblastoma 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 1 \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Wilms Tumor Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Neoplasm ∟ Genes, Tumor Suppressor ∟ Genes, Retinoblastoma 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 1 \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Wilms Tumor Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Retinoblastoma 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 1 \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Wilms Tumor X
Broader terms:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Inheritance Patterns ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Retinoblastoma Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Neoplasm ∟ Genes, Tumor Suppressor ∟ Genes, Retinoblastoma Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Retinoblastoma Genes, Tumor Suppressor > Genes, Recessive > Inheritance Patterns > Genetic Phenomena > Medical Subject Headings (MeSH) Genes, Tumor Suppressor > Genes, Neoplasm > Genes > Genome Components > Genome > Genetic Structures > Medical Subject Headings (MeSH) Genes, Tumor Suppressor > Genes, Recessive > Genes > Genome Components > Genome > Genetic Structures > Medical Subject Headings (MeSH) X
History note:	Retinoblastoma/genetics (1972-1990)X
historyNote*:	91 X
publicMeSHNote*:	91 X
Scope note:	Tumor suppressor genes located on human chromosome 13 in the region 13q14 and coding for a family of phosphoproteins with molecular weights ranging from 104 kDa to 115 kDa. One copy of the wild-type Rb gene is necessary for normal retinal development. Loss or inactivation of both alleles at this locus results in retinoblastoma. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1990-05-07X
dateEstablished*:	1991-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	AGSX
Type:	Concept X
Coordinate terms:	Genes, APC \| Genes, BRCA1 \| Genes, BRCA2 \| Genes, DCC \| Genes, MCC \| Genes, Neurofibromatosis 1 \| Genes, Neurofibromatosis 2 \| Genes, p16 \| Genes, p53 \| Genes, Wilms Tumor X
URI:	X
Labels and equivalent concepts:	Retinoblastoomageenit (fi) Retinoblastoomageeni (fi, replaced) Retinoblastomgener (sv) Gener, retinoblastom (sv, replaced) Rb-gener (sv, replaced) Retinoblastoma Genes (en, replaced) Rb Genes (en, replaced) Genes, Rb (en, replaced) X
Share:	X