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trigonocephaly 1

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Any isolated trigonocephaly in which the cause of the disease is a mutation in the FGFR1 gene.
Uniprot Description A keel-shaped deformation of the forehead, caused by premature fusion of the metopic sutures. It results in a triangular shape of the head.
Mondo Term and Equivalent IDs
MONDO:0008603:  trigonocephaly 1