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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
MESH:C566511: 
Orphanet:168624: 
UMLS:C1865070: