Disease #05364 (GPIBD15 (glycosylphosphatidylinositol biosynthesis defect, type 15 (GPIBD-15)), OMIM:617810)

Official abbreviation GPIBD15
Name glycosylphosphatidylinositol biosynthesis defect, type 15 (GPIBD-15)
OMIM ID 617810
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GPAA1
Associated tissues -
Disease features -
Remarks -
Date created 2017-12-29 14:39:07 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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