| Condition | Inheritance Pattern | Gene |
|---|---|---|
| Marfan Syndrome | Autosomal Dominant | FBN1 |
| Simple Ectopia Lentis | Autosomal Dominant | FBN1 |
| Ehlers-Danlos Syndrome (classical type) | Autosomal Dominant | COL5A1 and COL5A2 |
| Homocystinuria | Autosomal Recessive | CS |
| Weill-Marchesani Syndrome | Autosomal Recessive | ADAMTS10 |
| WM-like Syndrome | Autosomal Recessive | ADAMTS17 |
| Knoblock syndrome | Autosomal Recessive | COL18A1 |
| Cohen Syndrome | Autosomal Recessive | COH1 |
| Megalocornea with ectopia lentis | Autosomal Recessive | LTBP2 |
| Ectopia lentis et pupillae | Autosomal Recessive | ADAMTSL4 |
| Ectopia lentis with filtering blebs | Autosomal Recessive | ASPH |
- Adapted from: Elias Traboulsi,MD,M.Ed University of Iowa Research Day Keynote Speaker 4/21/2017
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