Disease #03462 (OI10 (osteogenesis imperfecta, type X (OI10)), OMIM:613848)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OI10
Name	osteogenesis imperfecta, type X (OI10)
OMIM ID	613848
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SERPINH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-05-16 13:12:31 +02:00 (CEST)

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