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Nephrolithiasis/osteoporosis, hypophosphatemic

MedGen UID:
Concept ID:
Disease or Syndrome
Synonym: nephrolithiasis/osteoporosis, hypophosphatemic
Related genes: NHERF1, SLC34A1
Monarch Initiative: MONDO:0000079
OMIM® Phenotypic series: PS612286

Recent clinical studies


Gordon RJ, Li D, Doyle D, Zaritsky J, Levine MA
J Clin Endocrinol Metab 2020 Jul 1;105(7):2392-400. doi: 10.1210/clinem/dgaa217. PMID: 32311027Free PMC Article

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