inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation

Findings

No curated finding names inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Where it sits

A kind of

• congenital disorder of glycosylation
• disorder of GPI anchor biosynthesis
• inherited lipid metabolism disorder

Narrower terms (8)

• CHIME syndrome
• GM3 synthase deficiency
• hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• hyperphosphatasia-intellectual disability syndrome
• intellectual disability, autosomal recessive 53
• multiple congenital anomalies-hypotonia-seizures syndrome 1
• multiple congenital anomalies-hypotonia-seizures syndrome 2
• multiple congenital anomalies-hypotonia-seizures syndrome 3

Resolves to: inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation

Also called

disorder of glycosphingolipid and GPI-anchored proteins glycosylation