Hypocalcemia with bartter syndrome
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Hypocalcemia, Autosomal Dominant, with Bartter Syndrome | C1832612 | CASR | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |