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Summary Literature (0)
MIM:613456 - FRONTONASAL DYSPLASIA 3; FND3

Xenbase Genes: alx1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013271 - frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome

Disease Ontology (DO):
DOID:0081047 - frontonasal dysplasia 3