| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 16q22.1 | Congenital disorder of glycosylation, type IIj | 613489 | AR | 3 |
| Saul-Wilson syndrome | 618150 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 16q22.1 | Saul-Wilson syndrome | 618150 | AD | 3 | COG4 | 606976 |
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