occasional neurofibromas Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Neurofibromas present in a smaller number than usually seen in neurofibromatosis type 1. (Human Phenotype Ontology, HP_0009595)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009595
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Genes

1 genes associated with the occasional neurofibromas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NF2 neurofibromin 2 (merlin)