Hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement | 2196 | CLDN19 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |