has material basis in germline mutation in FBN1 Weill-Marchesani syndrome 2, dominant https://github.com/monarch-initiative/mondo/issues/4948 https://www.malacards.org/card/weill_marchesani_syndrome_2 GEMSS A Weill-Marchesani syndrome characterized by progressive joint stiffness, glaucoma, short stature and lens dislocation. It has been described in three members of a family (the grandfather, his daughter and grandson). It is likely to be transmitted as an autosomal dominant trait. The acronym GEMSS (Glaucoma, Ectopia, Microspherophakia, Stiff joints, Short stature) was proposed as a name for the syndrome. This syndrome shows similarities to Moore-Federman syndrome. glaucoma, ectopia, microspherophakia, Stiff joints and short stature syndrome Weill-Marchesani syndrome type 2 MONDO:0012013 UMLS:C1869115 Weill-Marchesani syndrome 2 spherophakia-brachymorphia syndrome SCTID:722450007 GARD:0002452 GEMSS syndrome MEDGEN:358388 OMIM:608328 Orphanet:2084 glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome Weill-Marchesani syndrome, autosomal dominant mesodermal Dysmorphodystrophy, congenital WMS2 Weill-Marchesani syndrome