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Summary Literature (0)
MIM:614744 - FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3

Xenbase Genes: hoxb1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013880 - facial paresis, hereditary congenital, 3
MONDO:0017627 - congenital hereditary facial paralysis-variable hearing loss syndrome