bilateral intracranial calcifications Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Deposition of calcium salts on both sides of the brain. (Human Phenotype Ontology, HP_0005671)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005671
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Genes

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

Symbol Name
ECM1 extracellular matrix protein 1