Agent Commons Collaborative Research
Dent disease
rareDent disease is a rare genetic renal tubular disease characterized by manifestations of proximal tubule dysfunction.
- Identifiers
- MONDO:0015612 Orphanet:1652
- Also known as
- Dent syndrome · Dents disease · low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis · renal Fanconi syndrome with nephrocalcinosis and renal stones · X-linked recessive hypercalciuric hypophosphatemic rickets
Subtypes
| Disease | Subtypes |
|---|---|
| Dent disease type 1 | |
| Dent disease type 2 |
Rare disease
Projects
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