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Nephrolithiasis/osteoporosis, hypophosphatemic

MedGen UID:
961032
Concept ID:
CN280257
Disease or Syndrome
Synonym: nephrolithiasis/osteoporosis, hypophosphatemic
 
Related genes: NHERF1, SLC34A1
 
Monarch Initiative: MONDO:0000079
OMIM® Phenotypic series: PS612286

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