Monarch Disease Ontology term MONDO_0018096 (Weill-Marchesani syndrome) (WMS) is a rare condition characterized by short stature, brachydactyly, joint stiffness, and characteristic eye abnormalities including microspherophakia, ectopia of the lens, severe myopia, and glaucoma. Also known as: Marchesani-Weill syndrome, Weill Marchesani Syndrome, congenital mesodermal dystrophy, mesodermal Dysmorphodystrophy, congenital, spherophakia brachymorphia syndrome, spherophakia-brachymorphia syndrome.