| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/608978 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the meacham syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| WT1 | Wilms tumor 1 |
