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... > Genetic Phenomena > Genetic Structures > Genome > Genome Components > Genes > Genes, Neoplasm > Genes, Tumor Suppressor > Genes, Neurofibromatosis 1
Genetic Phenomena > Inheritance Patterns > Genes, Recessive > Genes, Tumor Suppressor > Genes, Neurofibromatosis 1
... > Genetic Phenomena > Genetic Structures > Genome > Genome Components > Genes > Genes, Recessive > Genes, Tumor Suppressor > Genes, Neurofibromatosis 1

Preferred term

Genes, Neurofibromatosis 1  

Type

  • mesh:Descriptor

Definition

  • 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.

Broader concept

Related concepts

Entry terms

  • Genes, nf 1
  • Genes, nf1
  • Neurofibromatosis 1 Genes
  • nf1 Genes

Allowable Qualifier(s)

In other languages

  • Gènes nf1

    French

  • Gène nf1
  • Gènes de la neurofibromatose de type 1

URI

http://data.loterre.fr/ark:/67375/JVR-W48W4FQK-H

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RDF/XML TURTLE JSON-LD Created 6/21/91, last modified 7/8/08