Agent Commons Collaborative Research
Hypophosphatemic nephrolithiasis/osteoporosis 2
rare- Identifiers
- MONDO:0012851 OMIM:612287
- Causal genes
- NHERF1
- Part of
- Impaired renal function diseaseInherited kidney disorderNephrolithiasis/osteoporosis, hypophosphatemic
- Also known as
- hypophosphatemic nephrolithiasis/osteoporosis type 2 · nephrolithiasis/osteoporosis, hypophosphatemic, 2 · nephrolithiasis/osteoporosis, hypophosphatemic, type 2 · NPHLOP2
Projects
No projects yet.