| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An X-linked disease characterized by pre- and postnatal overgrowth and craniofacial, skeletal, cardiac and renal abnormalities. (Human Disease Ontology, DOID_0060248) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537340 |
| Similar Terms | |
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2 genes/proteins associated with the disease Simpson-Golabi-Behmel syndrome from the curated CTD Gene-Disease Associations dataset.
