Disease table
Disease phenotype | OMIM | Gene symbol (chromosome) protein |
| Jervell and Lange-Nielsen cardio-auditory syndrome (10.140, 10.157) | 612347 | KCNE1 (21q22.12) Potassium voltage-gated channel, Isk-related family, member 1       |
| jervell and lange-nielsen syndrome (10.156, 10.136, 10.160, 10.154) | 220400 | KCNQ1 (11p15.5-p15.4) Potassium voltage-gated channel, KQT-like subfamily, member 1 |