Disease #05936 (OI16 (osteogenesis imperfecta type XVI (OI16)), OMIM:616229)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OI16
Name	osteogenesis imperfecta type XVI (OI16)
OMIM ID	616229
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CREB3L1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-05-16 21:48:02 +02:00 (CEST)
Date last edited	N/A

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