| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 15q21.1 | Acromicric dysplasia | 102370 | AD | 3 |
| Ectopia lentis, familial | 129600 | AD | 3 | |
| Geleophysic dysplasia 2 | 614185 | AD | 3 | |
| Marfan lipodystrophy syndrome | 616914 | AD | 3 | |
| Marfan syndrome | 154700 | AD | 3 | |
| MASS syndrome | 604308 | AD | 3 | |
| Stiff skin syndrome | 184900 | AD | 3 | |
| Weill-Marchesani syndrome 2, dominant | 608328 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 15q21.1 | Marfan syndrome | 154700 | AD | 3 | FBN1 | 134797 |
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