|
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

MONDO:0013679 - inner canthus of right eye |
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)