- OMIM ID
-
601471
- OMIM term:
- FACIAL PARESIS, HEREDITARY CONGENITAL, 1; HCFP1
- Alternative terms:
-
FACIAL PALSY, CONGENITAL, UNILATERAL OR BILATERAL
MOEBIUS SYNDROME 2, FORMERLY; MBS2, FORMERLY
MOBIUS SYNDROME 2, FORMERLY
- (∗) Location:
- 3q21-q22
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
Loading mouse genes ...