Disease: Trigonocephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		0.700 GermlineCausalMutation disease ORPHANET Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. 21931569 2011
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		0.700 Biomarker disease HPO
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		0.700 Biomarker disease CTD_human
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		0.700 Biomarker disease GENOMICS_ENGLAND