| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An autosomal genetic disease characterized by short stature, bachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities. (Human Disease Ontology, DOID_0050475) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D056846 |
| Similar Terms | |
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2 genes/proteins associated with the disease Weill-Marchesani Syndrome from the curated CTD Gene-Disease Associations dataset.
