Preferred Label : FG syndrome;
ICD-11 definition : FG syndrome (FGS) is aX-linked recessive multiple congenital anomalies (MCA) and developmental
delay syndrome with a characteristic psychological pattern (delayed development of
sensory integration, attention deficit disorder, self-absorption and fascinations
with mechanical toys and objects). Males are affected, but carrier girls and women
may also be affected, sometimes more severely than the males.;
ICD-11 synonym : Keller syndrome; Opitz-Kaveggia syndrome;
Origin ID : 156523187;
Currated CISMeF NLP mapping
Validated automatic mappings to BTNT
FG syndrome (FGS) is aX-linked recessive multiple congenital anomalies (MCA) and developmental
delay syndrome with a characteristic psychological pattern (delayed development of
sensory integration, attention deficit disorder, self-absorption and fascinations
with mechanical toys and objects). Males are affected, but carrier girls and women
may also be affected, sometimes more severely than the males.