Trigonocephaly 1

MONDO:0008603

Any isolated trigonocephaly in which the cause of the disease is a mutation in the FGFR1 gene.

Also known as: FGFR1 isolated trigonocephaly, isolated trigonocephaly caused by mutation in FGFR1, trigonocephaly 1, trigonocephaly type 1, TRIGNO1, craniosynostosis, metopic

35 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by