|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the FG syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|MED12||mediator complex subunit 12|