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familial scaphocephaly syndrome, McGillivray type
Disease Summary
Associated Targets (1)
Tclin
1
Mondo Description Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.
Mondo Term and Equivalent IDs
MONDO:0012307: familial scaphocephaly syndrome, McGillivray type