Disease #05933 (OI18 (osteogenesis imperfecta, type XVIII (OI18)), OMIM:617952)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	OI18
Name	osteogenesis imperfecta, type XVIII (OI18)
OMIM ID	617952
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FAM46A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-05-12 07:29:17 +02:00 (CEST)
Date last edited	N/A

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