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Summary Literature (1)
OMIM:182212 - SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS


In Disease Ontology (DO):
DOID:2340 - craniosynostosis

In Mondo Disease Ontology:
MONDO:0008426 - Shprintzen-Goldberg syndrome

Human Disease Resources: OMIM

Xenbase Genes: fbn1, ski