Autosomal dominant hypophosphatemic rickets Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Autosomal dominant hypophosphatemic rickets (ADHR) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia. (Orphanet Rare Disease Ontology, Orphanet_89937)
External Link http://www.omim.org/entry/193100
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Genes

1 genes associated with the Autosomal dominant hypophosphatemic rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
FGF23 fibroblast growth factor 23