| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A genetic disease that is characterized by slow growth before and after birth, intellectual disability that is usually severe to profound, skeletal abnormalities involving the arms and hands, and distinctive facial features. (Human Disease Ontology, DOID_11725) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D003635 |
| Similar Terms | |
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3 genes/proteins associated with the disease De Lange Syndrome from the curated CTD Gene-Disease Associations dataset.
