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Disease association ontology term - MONDO:0009805 - osteogenesis imperfecta type 9

Term summary

ID
MONDO:0009805
Name
osteogenesis imperfecta type 9
Ontology or CV name
Disease association
Definition
Any osteogenesis imperfecta in which the cause of the disease is a mutation in the PPIB gene.

Parents

Annotation

Disease association

MONDO:0009805 - osteogenesis imperfecta type 9

References:

Genes: