Disease #03855 (OI15 (osteogenesis imperfecta, type XV (OI15)), OMIM:615220)

Official abbreviation OI15
Name osteogenesis imperfecta, type XV (OI15)
OMIM ID 615220
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene WNT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-05-16 21:50:02 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00434939 Pat1 PubMed: Zhu 2023 - F ? ? (unknown) - >08y06m - - - OI15 - WNT1 WNT1 2 1 Kim Worring
00435095 Pat1 PubMed: Çavdartepe 2023 - F yes Iraq - >07y - - - OI15 - - WNT1 1 2 Kim Worring
00435096 Pat2 PubMed: Çavdartepe 2023 - M yes Iraq - >05y - - - OI15 - - WNT1 1 1 Kim Worring
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