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Summary Literature (1)
DOID:0060757 - sclerosteosis 2

Disease Ontology Definition:A sclerosteosis that has_material_basis_in heterozygous or homozygous mutation in the LRP4 gene on chromosome 11p11.

Synonyms: SOST2

Xenbase Genes : lrp4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013679 - inner canthus of right eye

MIM:
MIM:614305 - SCLEROSTEOSIS 2; SOST2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), sclerosteosis (is_a)