Preferred Label : Filippi syndrome;
ICD-11 definition : Filippi syndrome is a genetic syndrome characterised by microcephaly, cutaneous syndactyly
of the fingers and toes, intellectual deficit, growth retardation and a characteristic
facies (high and broad nasal bridge, thin alae nasi, micrognathia and a high frontal
hairline).;
Origin ID : 1989471300;
Currated CISMeF NLP mapping
Filippi syndrome is a genetic syndrome characterised by microcephaly, cutaneous syndactyly
of the fingers and toes, intellectual deficit, growth retardation and a characteristic
facies (high and broad nasal bridge, thin alae nasi, micrognathia and a high frontal
hairline).
