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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 12p12.1 | ?Atrial fibrillation, familial, 12 | 614050 | AD | 3 |
| Cardiomyopathy, dilated, 1O | 608569 | AD | 3 | |
| Hypertrichotic osteochondrodysplasia (Cantu syndrome) | 239850 | AD | 3 | |
| Intellectual disability and myopathy syndrome | 619719 | AR | 3 |
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|
|
|
| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 12p12.1 | Hypertrichotic osteochondrodysplasia (Cantu syndrome) | 239850 | AD | 3 | ABCC9 | 601439 |
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