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

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Craniosynostosis (15) Human disease (14) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2) Isolated craniosynostosis (1)

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