Facial paresis, hereditary congenital - CISMeF

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CISMeF

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Facial paresis, hereditary congenitalOMIM phenotypic series

Preferred Label : Facial paresis, hereditary congenital;

Details

Origin ID

PS601471;

Automatic exact mappings (from CISMeF team)
- Facial paresis, hereditary, congenital [MeSH concept]
- facial paresis, hereditary, congenital [MeSH Supplementary Concept]

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25/05/2025

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