has material basis in germline mutation in FGFR2 familial scaphocephaly syndrome, McGillivray type https://www.malacards.org/card/familial_scaphocephaly_syndrome_mcgillivray_type https://www.malacards.org/card/scaphocephaly_maxillary_retrusion_and_impaired_intellectual_development OMIM:609579 MONDO:0012307 scaphocephaly-macrocephaly-maxillary retrusion-intellectual disability syndrome icd11.foundation:512057922 MESH:C566511 MEDGEN:355365 GARD:0003426 UMLS:C1865070 scaphocephaly, maxillary retrusion, and intellectual disability Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability. Orphanet:168624 scaphocephaly, maxillary retrusion, and mental retardation familial scaphocephaly syndrome