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| MASS syndrome, 604308 (3): Located in omimdefinitions
| Weill-Marchesani syndrome 2, dominant, 608328 (3): Located in omimdefinitions
| * 134797 FIBRILLIN 1| FBN1: Located in omimdefinitions
| Stiff skin syndrome, 184900 (3): Located in omimdefinitions
| Acromicric dysplasia, 102370 (3): Located in omimdefinitions
| Geleophysic dysplasia 2, 614185 (3): Located in omimdefinitions
| [Skin/hair/eye pigmentation 4, fair/dark skin], 113750 (3): Located in omimdefinitions
| * 609802 SOLUTE CARRIER FAMILY 24 (SODIUM/POTASSIUM/CALCIUM EXCHANGER), MEMBER: Located in omimdefinitions
| Spastic paraplegia 11, autosomal recessive, 604360 (3): Located in omimdefinitions
| Spastic paraplegia 51, autosomal recessive, 613744 (3): Located in omimdefinitions

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