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DO Term : osteogenesis imperfecta type 6 [DOID:0110350] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINF1 gene on chromosome 17p13.3.

synonyms:
OI6,
GARD:8700,
osteogenesis imperfecta type VI,
OMIM:613982,
ICD10CM:Q78.0,
613982

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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