Disease #05891 (OI20 (osteogenesis imperfecta, type XX (OI20)), OMIM:618644)

Official abbreviation OI20
Name osteogenesis imperfecta, type XX (OI20)
OMIM ID 618644
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MESDC2
Associated tissues -
Disease features -
Remarks -
Date created 2021-01-12 17:22:55 +01:00 (CET)
Date last edited N/A


Individuals

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00434981 Pat1 PubMed: Ghosh 2023 - F no India South Indian >08y - - - OI20 - - MESDC2 1 1 Kim Worring
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