Disease #03463 (OI12 (osteogenesis imperfecta, type XII (OI12)), OMIM:613849)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OI12
Name	osteogenesis imperfecta, type XII (OI12)
OMIM ID	613849
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SP7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-05-16 13:20:06 +02:00 (CEST)

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