Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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 - Worth syndrome

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