Disease #04672 (OI17 (osteogenesis imperfecta, type XVII (OI17)), OMIM:616507)

Official abbreviation OI17
Name osteogenesis imperfecta, type XVII (OI17)
OMIM ID 616507
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SPARC
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-05-16 13:25:25 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00435093 Pat1 PubMed: Anna Durkin 2022 - F no Slovakia (Slovak Republic) - >19y - - - OI17 - - SPARC 1 1 Kim Worring
00435094 Pat2 PubMed: Anna Durkin 2022 - M yes Iraq Kurdistan >11y - - - OI17 - - SPARC 1 1 Kim Worring
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