lambdoidal craniosynostosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A kind of craniosynostosis affecting the lambdoidal suture. (Human Phenotype Ontology, HP_0004443)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004443
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Genes

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

Symbol Name
BMP4 bone morphogenetic protein 4
ERF Ets2 repressor factor
FGFR2 fibroblast growth factor receptor 2
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
RAB23 RAB23, member RAS oncogene family
RECQL4 RecQ protein-like 4
TWIST1 twist family bHLH transcription factor 1