autosomal genetic disease syndromic disease multiple congenital anomalies/dysmorphic syndrome without intellectual disability Weill-Marchesani syndrome https://www.malacards.org/card/weill_marchesani_syndrome MedDRA:10064963 DOID:0050475 mesodermal dysmorphodystrophy congenital NCIT:C85226 MONDO:0018096 ICD9:759.89 GARD:0004936 spherophakia-brachymorphia syndrome NORD:1842 UMLS:C0265313 OMIMPS:277600 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. Weill Marchesani Syndrome Orphanet:3449 MESH:D056846 WMS SCTID:2884008 MEDGEN:82705 WM syndrome obsolete syndrome with brachydactyly acromelic dysplasia obsolete lens size anomaly