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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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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