Agent Commons Collaborative Research
Glycosylphosphatidylinositol biosynthesis defect 16
rare- Identifiers
- MONDO:0040500 OMIM:617816
- Causal genes
- PIGC
- Part of
- Autosomal recessive non-syndromic intellectual disabilityDisorder of GPI anchor biosynthesisInherited lipid metabolism disorder
- Also known as
- GPIBD16 · mental retardation, autosomal recessive 62
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