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FG syndrome 2

Disease Summary
Associated Targets (3)
Tbio

2

Tchem

1


Explore Associated Targets
Mondo Description Any FG syndrome in which the cause of the disease is a mutation in the FLNA gene.
Uniprot Description FG syndrome (FGS) is an X-linked disorder characterized by mental retardation, relative macrocephaly, hypotonia and constipation.
Mondo Term and Equivalent IDs
MONDO:0010297:  FG syndrome 2
GARD:0009923: 
UMLS:C1845902: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found