|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||Meacham syndrome is a multiple malformation syndrome characterized by congenital diaphragmatic abnormalities, genital defects and cardiac malformations. (Orphanet Rare Disease Ontology, Orphanet_3097)|
|Downloads & Tools|
1 genes associated with the Meacham syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|WT1||Wilms tumor 1|