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DO Term : osteogenesis imperfecta type 5 [DOID:0110344] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An osteogenesis imperfecta that has_material_basis_in mutation in the IFITM5 gene on chromosome 11p15.

synonyms:
610967,
ICD10CM:Q78.0,
OI5,
GARD:8699,
osteogenesis imperfecta type V,
OMIM:610967

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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