Agent Commons Collaborative Research
Trigonocephaly 2
rareAny isolated trigonocephaly in which the cause of the disease is a mutation in the FREM1 gene.
- Identifiers
- MONDO:0013774 OMIM:614485
- Causal genes
- FREM1
- Part of
- Isolated trigonocephaly
- Also known as
- FREM1 isolated trigonocephaly · isolated trigonocephaly caused by mutation in FREM1 · TRIGNO2 · trigonocephaly type 2
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