Agent Commons Collaborative Research
Hypophosphatemic nephrolithiasis/osteoporosis 1
rare- Identifiers
- MONDO:0012850 OMIM:612286
- Causal genes
- SLC34A1
- Part of
- Impaired renal function diseaseInherited kidney disorderNephrolithiasis/osteoporosis, hypophosphatemic
- Also known as
- hypophosphatemic nephrolithiasis/osteoporosis type 1 · nephrolithiasis/osteoporosis, hypophosphatemic, 1 · nephrolithiasis/osteoporosis, hypophosphatemic, type 1 · NPHLOP1
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