Disease association ontology term - MONDO:0030861 - osteogenesis imperfecta, type 21

Term summary

ID: MONDO:0030861
Name: osteogenesis imperfecta, type 21
Ontology or CV name: Disease association

Parents

is_a osteogenesis imperfecta

Annotation

Disease association

MONDO:0030861 - osteogenesis imperfecta, type 21

References:

PB_REF:0000006

Genes:

erd2 (SPBP8B7.22)