fg syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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)
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Genes

4 genes involed in the disease fg syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
FLNA filamin A, alpha
MED12 mediator complex subunit 12
UPF3B UPF3 regulator of nonsense transcripts homolog B (yeast)