abnormality of the falx cerebri Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the Falx cerebri. (Human Phenotype Ontology, HP_0010653)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010653
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6 genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
COL11A1 collagen, type XI, alpha 1
DDR2 discoidin domain receptor tyrosine kinase 2
PTCH1 patched 1
PTCH2 patched 2
SUFU suppressor of fused homolog (Drosophila)