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, Wilms Tumor

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Inheritance Patterns ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Wilms Tumor 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 1 \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Retinoblastoma Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Neoplasm ∟ Genes, Tumor Suppressor ∟ Genes, Wilms Tumor 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 1 \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Retinoblastoma Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Wilms Tumor 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 1 \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Retinoblastoma X
Broader terms:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Inheritance Patterns ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Wilms Tumor Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Neoplasm ∟ Genes, Tumor Suppressor ∟ Genes, Wilms Tumor Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Wilms Tumor 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
historyNote*:	91 X
publicMeSHNote*:	91 X
Scope note:	Genes at loci that are involved in the development of WILMS TUMOR. Included are human WT1 at 11p13 and human WT2 (MTACR1) at 11p15. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1990-05-07X
dateEstablished*:	1991-01-01X
dateRevised*:	2005-07-01X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	AGSX
Related term:	Beckwith-Wiedemann Syndrome \| Denys-Drash Syndrome \| WAGR Syndrome \| Wilms Tumor \| WT1 Proteins X
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, Retinoblastoma X
URI:	X
Labels and equivalent concepts:	Nefroblastoomaa aiheuttavat geenit (fi) Wilmsin kasvainta aiheuttava geeni (fi, replaced) Nefroblastoomageenit (fi, replaced) Nefroblastoomageeni (fi, replaced) Wilmsin kasvainta aiheuttavat geenit (fi, replaced) Wilmsin tuumoria aiheuttava geeni (fi, replaced) Wilmsin tuumoria aiheuttavat geenit (fi, replaced) Nefroblastoomaa aiheuttava geeni (fi, replaced) Wilms tumör-gener (sv) Gener, Wilms tumör (sv, replaced) WT2 Genes, Human (en, replaced) MTACR1 Genes (en, replaced) Genes, Wilms' (en, replaced) Multiple Tumor-Associated Chromosome Region 1 Genes (en, replaced) Wilms Tumor Genes (en, replaced) WT1 Genes, Human (en, replaced) Wilms' Tumor Genes (en, replaced) Genes, Wilms (en, replaced) X
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