FG syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An X-linked disease characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern. (Human Disease Ontology, DOID_14711)
External Link http://www.omim.org/entry/305450
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Genes

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

Symbol Name
MED12 mediator complex subunit 12