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Summary Literature (1)
MIM:309000 - LOWE OCULOCEREBRORENAL SYNDROME; OCRL

Xenbase Genes: ocrl

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010645 - oculocerebrorenal syndrome

Disease Ontology (DO):
DOID:1056 - oculocerebrorenal syndrome