Any syndromic craniosynostosis in which the cause of the disease is a mutation in the TCF12 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
Crouzon syndrome
MONDO:0007405
Beare-Stevenson cutis gyrata syndrome
MONDO:0007412
Shprintzen-Goldberg syndrome
MONDO:0008426
acrocephalopolydactyly
MONDO:0008709
Antley-Bixler syndrome
MONDO:0008803
C syndrome
MONDO:0008893