osteogenesis imperfecta type 16

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Summary

Literature (0)

DOID:0110345 - osteogenesis imperfecta type 16

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in contiguous gene deletion on chromosome 11p11.

Synonyms: chromosome 11p11.2 deletion syndrome 91.3-KB, OI16, osteogenesis imperfecta type XVI

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: creb3l1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014544 - osteogenesis imperfecta type 16

MONDO:0014544 - osteogenesis imperfecta type 16

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)