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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,
Echinobase Genes : wnt1
MIM:615220 - osteogenesis imperfecta, type xv; oi15 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
osteogenesis imperfecta (is_a)