HFM, Hemifacial microsomia, 170474

N. diseases: 22; N. variants: 0
Disease: Dysmorphism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1737329
Disease: Dysmorphism
Dysmorphism 		0.010 Biomarker disease BEFREE Hemifacial microsomia (HFM) is a common birth defect involving first and second branchial arch derivatives.The phenotype is extremely variable. 11810276 2001