| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| 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) |
| Similar Terms | |
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2 genes involed in the disease weill-marchesani syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
