FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term multiple synostoses syndrome ID (Ontology) DOID:0050794 (Human Disease)
Definition A dysostosis that is characterized by characterized by multiple joint fusions, usually commencing in the hands, conductive deafness, and characteristic facial features, including a broad, tubular-shaped nose and a thin upper vermilion.
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Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
bone development disease        |
 |__dysostosis__________________|
                                multiple synostoses syndrome  1 rec.
                                 |__multiple synostoses syndrome 1
                                 |__multiple synostoses syndrome 2
                                 |__multiple synostoses syndrome 3 1 rec.
                                 |__multiple synostoses syndrome 4
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Is a autosomal dominant disease
dysostosis
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MIM:PS186500
ORDO:3237