- OMIM ID
-
604185
- OMIM term:
- FACIAL PARESIS, HEREDITARY CONGENITAL, 2; HCFP2
- Alternative terms:
-
MOEBIUS SYNDROME 3, FORMERLY; MBS3, FORMERLY
MOBIUS SYNDROME 3, FORMERLY
- (∗) Location:
- 10q21.3-q22.1
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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