Disease #05401 (GPIBD16 (glycosylphosphatidylinositol biosynthesis defect, type 16 (GPIBD-16)), OMIM:617816)

Official abbreviation	GPIBD16
Name	glycosylphosphatidylinositol biosynthesis defect, type 16 (GPIBD-16)
OMIM ID	617816
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PIGC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2018-03-09 08:24:14 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD