Disease #02999 (OI11 (osteogenesis imperfecta type XI (OI11)), OMIM:610968)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OI11
Name	osteogenesis imperfecta type XI (OI11)
OMIM ID	610968
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FKBP10
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-05-16 09:09:05 +02:00 (CEST)

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