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Disease association ontology term - MONDO:0024321 - disorder of GPI anchor biosynthesis

Term summary

ID
MONDO:0024321
Name
disorder of GPI anchor biosynthesis
Ontology or CV name
Disease association
Definition
A disease that has its basis in the disruption of GPI anchor biosynthetic process.

Parents

Annotation

Disease association

MONDO:0010221 - CHIME syndrome

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MONDO:0033364 - developmental and epileptic encephalopathy, 55

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MONDO:0032808 - developmental and epileptic encephalopathy, 77

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MONDO:0032822 - developmental and epileptic encephalopathy, 80

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MONDO:0060627 - glycosylphosphatidylinositol biosynthesis defect 15

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MONDO:0040500 - glycosylphosphatidylinositol biosynthesis defect 16

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MONDO:0060724 - glycosylphosphatidylinositol biosynthesis defect 17

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MONDO:0029140 - glycosylphosphatidylinositol biosynthesis defect 18

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MONDO:0012465 - hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency

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MONDO:0009398 - hyperphosphatasia with intellectual disability syndrome 1

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MONDO:0013882 - hyperphosphatasia with intellectual disability syndrome 2

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MONDO:0014318 - hyperphosphatasia with intellectual disability syndrome 4

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MONDO:0014457 - hyperphosphatasia with intellectual disability syndrome 5

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MONDO:0014780 - hyperphosphatasia with intellectual disability syndrome 6

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MONDO:0014832 - intellectual disability, autosomal recessive 53

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MONDO:0013563 - multiple congenital anomalies-hypotonia-seizures syndrome 1

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MONDO:0010466 - multiple congenital anomalies-hypotonia-seizures syndrome 2

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MONDO:0014165 - multiple congenital anomalies-hypotonia-seizures syndrome 3

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MONDO:0030037 - neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures

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MONDO:0010438 - paroxysmal nocturnal hemoglobinuria 1

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MONDO:0014166 - paroxysmal nocturnal hemoglobinuria 2

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