Disease #02928

Official abbreviation GPID;GPIBD-1
Name glycosylphosphatidylinositol deficiency (GPID, glycosylphosphatidylinositol deficiency, type 1 (GPIBD-1))
OMIM ID 610293
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PIGM
Associated tissues -
Disease features autosomal recessive
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00025010 - PubMed: Almeida 2006 2 unrelated kindreds, Middle Eastern and Turkish origin - yes United Kingdom (Great Britain) Middle Eastern; Turkish - 0 - - GPID;GPIBD-1 propensity to portal venous thrombosis and seizures PIGM PIGM 1 1 Philippe Campeau
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