Glycosylphosphatidylinositol Biosynthesis Defect 25 (GPIBD25)

Alias:
Neurodevelopmental Disorder with Hypotonia and Contractures
Gpibd25
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Glycosylphosphatidylinositol Biosynthesis Defect 25, also known as neurodevelopmental disorder with hypotonia and contractures, is related to cerebellar atrophy, developmental delay, and seizures and glucosephosphate isomerase deficiency. An important gene associated with Glycosylphosphatidylinositol Biosynthesis Defect 25 is C18orf32 (Chromosome 18 Open Reading Frame 32). Affiliated tissues include brain and eye, and related phenotypes are hypotonia and coarse hair
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
3
1

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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