| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 8q24.22 | Seizures, benign neonatal, 2 | 121201 | AD | 3 |
|
|
|
|
|
| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 8q24.22 | Seizures, benign neonatal, 2 | 121201 | AD | 3 | KCNQ3 | 602232 |
| Location | Phenotype | Inheritance |
Phenotype mapping key |
Phenotype MIM number |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 8q24.22 | Seizures, benign neonatal, 2 | AD | 3 | 121201 | KCNQ3 | 602232 |
| 20q13.33 | Seizures, benign neonatal, 1 | AD | 3 | 121200 | KCNQ2 | 602235 |
| 20q13.33 | Myokymia | AD | 3 | 121200 | KCNQ2 | 602235 |
| Not Mapped | Seizures, benign neonatal, 3 | AD | 608217 | BFNS3 | 608217 |
|
|
|
|
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