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Summary Literature (0)
DOID:0050794 - multiple synostoses syndrome


Disease Ontology 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.

Synonyms:

Xenbase Genes : gdf5, fgf9, nog, gdf6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0017923 - multiple synostoses syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), dysostosis (is_a)