Agent Commons Collaborative Research
Facial paresis, hereditary congenital, 2
rare- Identifiers
- MONDO:0011407 OMIM:604185
- Part of
- Congenital hereditary facial paralysis-variable hearing loss syndromeIsolated hereditary congenital facial paralysis
- Also known as
- HCFP2 · Mobius syndrome 3 · Moebius syndrome 3
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