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Summary Literature (0)
DOID:0110347 - osteogenesis imperfecta type 15


Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the WNT1 gene on chromosome 12q13.

Synonyms: OI15, osteogenesis imperfecta type XV

Referenced OMIM:
OMIM:615220 - OSTEOGENESIS IMPERFECTA, TYPE XV; OI15

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : wnt1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): osteogenesis imperfecta (is_a)


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Version: 4.15.0
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