neurofibromas Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of multiple cutaneous neurofibromas. (Human Phenotype Ontology, HP_0001067)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001067
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Genes

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

Symbol Name
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
NF1 neurofibromin 1
NF2 neurofibromin 2 (merlin)
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SPRED1 sprouty-related, EVH1 domain containing 1