Preferred Label : Familial scaphocephaly syndrome, McGillivray type;
ICD-11 definition : Familial scaphocephaly syndrome, McGillivray type is a rare craniosynostosis syndrome
characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild
intellectual disability.;
Origin ID : 512057922;
Currated CISMeF NLP mapping
Familial scaphocephaly syndrome, McGillivray type is a rare craniosynostosis syndrome
characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild
intellectual disability.