Facial Paresis, Hereditary Congenital, 2 (HCFP2)

Alias:

Facial Paresis, Hereditary, Congenital

Moebius Syndrome 3, Formerly

Mobius Syndrome 3, Formerly

Mbs3, Formerly

Hcfp2

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Facial Paresis, Hereditary Congenital, 2, is also known as facial paresis, hereditary, congenital. An important gene associated with Facial Paresis, Hereditary Congenital, 2 is MBS2 (Moebius Syndrome 2). Related phenotypes are facial palsy and hearing impairment

Related ID：

MALACARDS：FCL050

OMIM：604185