hemifacial microsomia Gene Set

Dataset	OMIM Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch. (Human Disease Ontology, DOID_2907)
External Link	http://www.omim.org/entry/164210
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Genes

1 genes associated with the hemifacial microsomia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol	Name
HFM	Hemifacial microsomia