Facial paresis, hereditary congenital, 3

Any congenital hereditary facial paralysis-variable hearing loss syndrome in which the cause of the disease is a mutation in the HOXB1 gene.

Also known as: HOXB1 congenital hereditary facial paralysis-variable hearing loss syndrome, congenital hereditary facial paralysis-variable hearing loss syndrome caused by mutation in HOXB1, facial paresis, hereditary congenital, 3, facial paresis, hereditary congenital, type 3, HCFP3

1 clinical trial for this condition and its sub-types, 0 tagged with Facial paresis, hereditary congenital, 3 itself.