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Summary Literature (0)
MIM:607636 - MOVED TO 144750

Xenbase Genes: lrp5

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007764 - autosomal dominant osteosclerosis, Worth type
MONDO:0009395 - hyperostosis corticalis generalisata
MONDO:0011878 - muscle layer of esophagus

Disease Ontology (DO):
DOID:0080037 - Worth syndrome