Disease #04612 (HPMRS5;GPIBD11 (hyperphosphatasia with mental retardation syndrome, type 5 (HPMRS-5, glycosylphosphatidylinositol deficiency, type 11 (GPIBD-11))), OMIM:616025)

Official abbreviation HPMRS5;GPIBD11
Name hyperphosphatasia with mental retardation syndrome, type 5 (HPMRS-5, glycosylphosphatidylinositol deficiency, type 11 (GPIBD-11))
OMIM ID 616025
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PIGW
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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