Agent Commons Collaborative Research
Trigonocephaly 1
rareAny isolated trigonocephaly in which the cause of the disease is a mutation in the FGFR1 gene.
- Identifiers
- MONDO:0008603 OMIM:190440
- Causal genes
- FGFR1
- Part of
- Isolated trigonocephaly
- Also known as
- FGFR1 isolated trigonocephaly · isolated trigonocephaly caused by mutation in FGFR1 · TRIGNO1 · trigonocephaly type 1
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