hyperphosphatasia with impaired intellectual development syndrome 5

Summary
Synonym
  • GPIBD11
  • HPMRS5
  • glycosylphosphatidylinositol biosynthesis defect 11
  • hyperphosphatasia with mental retardation syndrome 5
Definition
A hyperphosphatasia with impaired intellectual development syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PIGW gene on chromosome 17q12.
Super Class
hyperphosphatasia with impaired intellectual development syndrome
External Links
Disease Ontology
DOID:0070432
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
284098 PIGW phosphatidylinositol glycan anchor biosynthesis class W
The Human Phenotype Ontology
Displaying entries 51 - 60 of 70 in total
HPO ID HPO Term
HP:0002714 Downturned corners of mouth
HP:0003155 Elevated circulating alkaline phosphatase concentration
HP:0006118 Shortening of all distal phalanges of the fingers
HP:0006808 Cerebral hypomyelination
HP:0008947 Infantile muscular hypotonia
HP:0010804 Tented upper lip vermilion
HP:0010850 EEG with spike-wave complexes
HP:0010864 Intellectual disability, severe
HP:0011471 Gastrostomy tube feeding in infancy
HP:0002521 Hypsarrhythmia
Displaying all 7 entries
Gene ID Gene Symbol Description
27315 PGAP2 post-GPI attachment to proteins 2
284098 PIGW phosphatidylinositol glycan anchor biosynthesis class W
55650 PIGV phosphatidylinositol glycan anchor biosynthesis class V
84720 PIGO phosphatidylinositol glycan anchor biosynthesis class O
84992 PIGY phosphatidylinositol glycan anchor biosynthesis class Y
93210 PGAP3 post-GPI attachment to proteins phospholipase 3
9487 PIGL phosphatidylinositol glycan anchor biosynthesis class L

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024