Disease #03504 (OI6 (osteogenesis imperfecta, type VI (OI6)), OMIM:613982)

Official abbreviation OI6
Name osteogenesis imperfecta, type VI (OI6)
OMIM ID 613982
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 SERPINF1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-05-16 12:55:18 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00326414 174848 - - M ? Syria - - - - - OI6 clinically osteogenesis imperfecta, multiple fractures of long tubular bones SERPINF1 SERPINF1 1 1 Andreas Laner
00410180 Pat3 PubMed: Kuptanon 2022, Journal: Kuptanon 2022 - M no Thailand - - - - - OI6 no Dentinogenesis imperfecta (-HP:0000703), no Blue sclerae (-HP:0000592), Short stature (HP:0004322) SERPINF1 SERPINF1 1 1 Thanakorn Theerapanon
00435097 Pat1 PubMed: Zhalsanova 2023 - M no Russia Tuva nationality >01y - - - OI6 - - SERPINF1 1 1 Kim Worring
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