| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Meacham syndrome is a multiple malformation syndrome characterized by congenital diaphragmatic abnormalities, genital defects and cardiac malformations. (Orphanet Rare Disease Ontology, Orphanet_3097) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C538162 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Meacham Winn Culler syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| WT1 | Wilms tumor 1 | 2.88009 |
