|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A metal metabolism disorder that results from the inactivation of hormone-like substances (phosphatonins) that promote phosphate excretion which has_material_basis_in a X-linked mutation in the PHEX gene. (Human Disease Ontology, DOID_0050445)|
|Downloads & Tools|
1 genes associated with the hypophosphatemic rickets, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
|PHEX||phosphate regulating endopeptidase homolog, X-linked|