DISEASES

Disease-gene associations mined from literature

Human genes for FG syndrome

FG syndrome [DOID:14711]

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.

Synonyms:  FG syndrome,  DOID:14711,  FG disease,  FG disorder,  Keller syndrome ...

Linkouts:  OMIM #1 #2 #3 #4 #5