| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 20p13 | Okur-Chung neurodevelopmental syndrome | 617062 | AD | 3 |
|
|
|
|
| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 20p13 | Okur-Chung neurodevelopmental syndrome | 617062 | AD | 3 | CSNK2A1 | 115440 |
|
|
|
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