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, Neurofibromatosis 1

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Inheritance Patterns ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Neurofibromatosis 1 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Retinoblastoma \| ∟ Genes, Wilms Tumor Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Neoplasm ∟ Genes, Tumor Suppressor ∟ Genes, Neurofibromatosis 1 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Retinoblastoma \| ∟ Genes, Wilms Tumor Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Neurofibromatosis 1 10 coordinate concepts ∟ Genes, APC \| ∟ Genes, BRCA1 \| ∟ Genes, BRCA2 \| ∟ Genes, DCC \| ∟ Genes, MCC \| ∟ Genes, Neurofibromatosis 2 \| ∟ Genes, p16 \| ∟ Genes, p53 \| ∟ Genes, Retinoblastoma \| ∟ Genes, Wilms Tumor X
Broader terms:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Inheritance Patterns ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Neurofibromatosis 1 Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Neoplasm ∟ Genes, Tumor Suppressor ∟ Genes, Neurofibromatosis 1 Medical Subject Headings (MeSH) ∟ Genetic Structures ∟ Genome ∟ Genome Components ∟ Genes ∟ Genes, Recessive ∟ Genes, Tumor Suppressor ∟ Genes, Neurofibromatosis 1 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:	Neurofibromatosis 1/genetics (1987-1991)X
historyNote*:	92 X
publicMeSHNote*:	92 X
Scope note:	Tumor suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1991-06-21X
dateEstablished*:	1992-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	AGSX
Related term:	Neurofibromatosis 1 \| Neurofibromin 1 X
Type:	Concept X
Coordinate terms:	Genes, APC \| Genes, BRCA1 \| Genes, BRCA2 \| Genes, DCC \| Genes, MCC \| Genes, Neurofibromatosis 2 \| Genes, p16 \| Genes, p53 \| Genes, Retinoblastoma \| Genes, Wilms Tumor X
URI:	X
Labels and equivalent concepts:	Neurofibromatoosi-1-geenit (fi) Neurofibromatoosi-1-geeni (fi, replaced) Neurofibromatos 1-gener (sv) Gener, neurofibromatos 1 (sv, replaced) nf1-gener (sv, replaced) nf1 Genes (en, replaced) Genes, nf1 (en, replaced) Neurofibromatosis 1 Genes (en, replaced) Genes, nf 1 (en, replaced) X
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