Any Pfeiffer syndrome in which the cause of the disease is a mutation in the FGFR2 gene.
Comprehensive, easy-to-understand information about this condition
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Pfeiffer syndrome type 1
MONDO:0019659
Pfeiffer syndrome type 2
MONDO:0019660
Pfeiffer syndrome type 3
MONDO:0019661
FGFR1-related Pfeiffer syndrome
MONDO:1060146