HFM, Hemifacial microsomia, 170474

N. diseases: 22; N. variants: 0
Disease: Congenital Abnormality ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.040 Biomarker group BEFREE Hemifacial microsomia (HFM) is a malformation characterized by asymmetric facial growth with mandibular and muscular involvement. 31187673 2019
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.040 Biomarker group BEFREE Hemifacial microsomia (HFM) is a common congenital malformation of the craniofacial region. 30205013 2018
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.040 Biomarker group BEFREE Hemifacial microsomia (HFM) is the second most common congenital craniofacial malformation. 29551253 2018
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.040 Biomarker group BEFREE Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome. 11810276 2001