Disorders

Frontonasal Dysplasia 1

Synonym(s): FND1, Frontonasal Malformation, Frontorhiny, Median Facial Cleft Syndrome

Gene	Locus	Protein
ALX3	1p13.3	Homeobox protein aristaless-like 3

Laboratory	Test Method	Prenatal	Carrier *
Boston Children's Hospital, Genetics Diagnostic Laboratory - Waltham, MA, USA

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.