Disease #05830 (GPIBD17 (glycosylphosphatidylinositol biosynthesis defect, type 17 (GPIBD17)), OMIM:618010)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	GPIBD17
Name	glycosylphosphatidylinositol biosynthesis defect, type 17 (GPIBD17)
OMIM ID	618010
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PIGH
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-09-11 12:47:02 +02:00 (CEST)
Date last edited	N/A

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