Facial paresis, hereditary congenital, 3

Definition

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 congenital hereditary facial paralysis-variable hearing loss syndrome caused by mutation in HOXB1, facial paresis, hereditary congenital, 3, facial paresis, hereditary congenital, type 3, HOXB1 congenital hereditary facial paralysis-variable hearing loss syndrome — per MONDO

Also identified as

• OMIM 614744 per MONDO
• UMLS C3553625 per MONDO