Disease #05934 (OI21 (osteogenesis imperfecta, type XXI (OI21)), OMIM:619131)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OI21
Name	osteogenesis imperfecta, type XXI (OI21)
OMIM ID	619131
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KDELR2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-05-16 21:32:09 +02:00 (CEST)
Date last edited	2021-05-16 21:39:27 +02:00 (CEST)

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