Disease #00637 (OI-2 (osteogenesis imperfecta, type II (OI-2)), OMIM:166210)

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	Curator: Johan T. den Dunnen

Official abbreviation	OI-2
Name	osteogenesis imperfecta, type II (OI-2)
OMIM ID	166210
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	COL1A1, COL1A2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A