low alkaline phosphatase Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally reduced serum levels of alkaline phosphatase activity. (Human Phenotype Ontology, HP_0003282)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003282
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Genes

2 genes associated with the low alkaline phosphatase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
SLC39A4 solute carrier family 39 (zinc transporter), member 4