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Summary Literature (0)
MIM:224750 - SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS

Xenbase Genes: wnt10a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009145 - pharyngeal region of foregut

Disease Ontology (DO):
DOID:0111647 - Schopf-Schulz-Passarge syndrome