Disease #02928 (GPIBD1 (glycosylphosphatidylinositol deficiency, type 1), OMIM:610293)

Official abbreviation GPIBD1
Name glycosylphosphatidylinositol deficiency, type 1
OMIM ID 610293
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PIGM
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00025010 - PubMed: Almeida 2006 2 unrelated kindreds, Middle Eastern and Turkish origin - yes United Kingdom (Great Britain) Middle Eastern; Turkish - - - - GPIBD1 propensity to portal venous thrombosis and seizures PIGM PIGM 1 1 Philippe Campeau
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