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Summary Literature (0)
MIM:616200 - RUIJS-AALFS SYNDROME; RJALS

Xenbase Genes: sprtn

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014527 - progeroid features-hepatocellular carcinoma predisposition syndrome

Disease Ontology (DO):
DOID:0111264 - Ruijs-Aalfs syndrome