Trigonocephaly 2

MONDO:0013774

Any isolated trigonocephaly in which the cause of the disease is a mutation in the FREM1 gene.

Also known as: FREM1 isolated trigonocephaly, isolated trigonocephaly caused by mutation in FREM1, trigonocephaly 2, trigonocephaly type 2, TRIGNO2, craniosynostosis, metopic

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

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