Disease #03752 (OI13 (osteogenesis imperfecta, type XIII (OI13)), OMIM:614856)

Official abbreviation OI13
Name osteogenesis imperfecta, type XIII (OI13)
OMIM ID 614856
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 BMP1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-05-12 13:22:32 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00410168 Pat1 PubMed: Kuptanon 2022, Journal: Kuptanon 2022 - M no Thailand - - - - - OI13 Dentinogenesis imperfecta (HP:0000703), no Blue sclerae (-HP:0000592), no Hearing abnormality (-HP:0000364) BMP1, COL1A1, COL1A2 BMP1 2 1 Thanakorn Theerapanon
00432477 Pat39 PubMed: Nadyrshina 2022 - M yes Russia Bashkir ethnicy >24y - - - OI13 - - P3H1 1 1 Kim Worring
00434910 Pat1 PubMed: Cao 2023 - F ? China - >05y - - - OI13 - - COL1A1 2 1 Kim Worring
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