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Summary Literature (0)
MIM:193300 - VON HIPPEL-LINDAU SYNDROME; VHLS

Xenbase Genes: vhl, ccnd1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008667 - von Hippel-Lindau disease

Disease Ontology (DO):
DOID:14175 - von Hippel-Lindau disease