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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

0 clinical trials for this condition and its sub-types, 0 tagged with Trigonocephaly 1 itself.

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