You are using an outdated browser. Please upgrade your browser to improve your experience.

FG syndrome 2

Disease Summary
Associated Targets (3)
Tbio

2

Tchem

1


GARD Rare
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: