Meacham syndrome Gene Set

Dataset ClinVar Gene-Phenotype 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
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Genes

1 genes associated with the Meacham syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
WT1 Wilms tumor 1