Disease #02998 (OI5 (osteogenesis imperfecta, type V (OI5)), OMIM:610967)

Official abbreviation OI5
Name osteogenesis imperfecta, type V (OI5)
OMIM ID 610967
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 8
Phenotype entries for this disease 6
Associated with 1 gene IFITM5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-05-16 09:24:20 +02:00 (CEST)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00361765 - - - - - - - - - - - OI5 Recurrent fractures, microphthalmia Developmental delay - SERPINF1, STRA6 2 1 Anju Shukla
00431388 patient PubMed: Wu 2020 - F no China - >00y - - - OI5 - - IFITM5 1 1 Kim Worring
00431420 Pat1 PubMed: Whyte 2020 - M no United States - >29y - - - OI5 - - IFITM5 1 1 Kim Worring
00431421 Pat2 PubMed: Whyte 2020 - F ? United States - 51y - - - OI5 - - IFITM5 1 1 Kim Worring
00431427 patient PubMed: Deng 2021 - M no China Han >14y - - pamidronate, zoledronate, vitamin A, vitamin D, calcium OI5 - - IFITM5 1 1 Kim Worring
00432478 Pat41 PubMed: Nadyrshina 2022 - F ? Russia - >26y - - - OI5 - - IFITM5 1 1 Kim Worring
00432479 Pat42 PubMed: Nadyrshina 2022 - M ? Russia - >10y - - - OI5 - - IFITM5 1 1 Kim Worring
00434127 Pat40 PubMed: Nadyrshina 2022 - F ? Russia - >27y - - - OI5 - - IFITM5 1 1 Kim Worring
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