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DO Term : osteogenesis imperfecta type 9 [DOID:0110349] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An osteogenesis imperfecta that has_material_basis_in mutation in the PPIB gene on chromosome 15q22.

synonyms:
OI9,
osteogenesis imperfecta type IX,
OMIM:259440,
259440,
GARD:10619,
ICD10CM:Q78.0

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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