Disease: Brachycephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.600 GermlineCausalMutation disease ORPHANET Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations. 17343269 2007
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.600 Biomarker disease CTD_human Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome. 12221714 2002
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.600 Biomarker disease HPO